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Abstract

Over the past 150 years, since Vogel in 1820 isolated the parent oxygen heterocycle, coumarin (1) from Coumarouna odorata = Dipteryx odorata (1), coumarins have been recognized as widely distributed plant products. The vast majority carry an oxygen substituent at C-7; consequently 7-hydroxycoumarin [umbelliferone, (2)], one of the most widely distributed coumarins, is often regarded as the parent, in a structural sense and also biogenetically, of a large number of the structurally more complex coumarins. A number of review articles on natural plant coumarins have appeared (154, 302, 344, 420, 525, 541, 548) since the last in this series (153), the most comprehensive, albeit dealing solely with coumarins of the Umbelliferae, being that of Nielsen in 1970 (419).

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References

  1. Abernethy, J. L.: The Historical and Current Interest in Coumarin. J. Chem. Ed. 46, 561 (1969).

    Google Scholar 

  2. Abu-Mustafa, E. A., F. K. A. El-Bay, and M. B. E. Fayez: Natural Coumarins. XIII. Structure of Majurin, a New Constituent of Ammi majus L. Fruits. Tetra­hedron Letters 1971, 1657.

    Google Scholar 

  3. Abu-Mustafa, E. A., F. K. A. El-Bay, and M. B. E. Fayez: Ammirin, a New Coumarin Constituent from Ammi majus L. Fruits. Naturwiss. 62, 39 (1975).

    CAS  Google Scholar 

  4. Abu-Mustafa, E. A., and M. B. E. Fayez: Natural Coumarins. I. Marmesin and Marmesinin, Further Products from the Fruits of Ammi majus L. J. Org. Chem. 26, 161 (1961).

    CAS  Google Scholar 

  5. Abyshev, A. Z.: Isogosferol, a New Furocoumarin from the Root of Prangos lophoptera. Khim. prirod. Soedinenii 10, 83 (1974); Chem. Abs. 80, 120816 (1974).

    Google Scholar 

  6. Abyshev, A. Z.: Structures of Components of the Roots of Prangos ferulacea. Khim. prirod. Soedinenii 10, 568 (1974; Chem. Abs. 82, 139897 (1975).

    Google Scholar 

  7. Abyshev, A. Z.: Coumarin Composition of the Roots, Stems and Fruit of Prangos lophoptera. Khim. prirod. Soedinenii 10, 708 (1974); Chem. Abs. 82, 135682 (1975).

    Google Scholar 

  8. Abyshev, A. Z.: Structure of Suberosin Transformation Products and their Possible Biogenesis. Khim. prirod. Soedinenii 11, 131 (1975); Chem. Abs. 83, 96944 (1975).

    Google Scholar 

  9. Abyshev, A. Z.: Structure of Lophopterol. Khim. prirod. Soedinenii 12, 253 (1976); Chem. Abs. 85, 59601 (1976).

    Google Scholar 

  10. Abyshev, A. Z., and I. V. Brodskii: Prandiol, a New Dihydrofurocoumarin from the Roots of Prangos biebersteinii. Khim. prirod. Soedinenii 10, 574 (1974); Chem. Abs. 82, 121643 (1975).

    Google Scholar 

  11. Abyshev, A. Z., I. V. Brodskii, and P. P. Denisenko: Coumarins of Prangos alata Grossh. — Prangos biebersteinii Karjag. Khim. prirod. Soedninenii 9, 269 (1973); Chem. Abs. 79,75844(1973).

    Google Scholar 

  12. Abyshev, A. Z., I. V. Brodskii, P. P. Denisenko, and A. I. Ermakov: The Structure of Alatol. Khim. prirod. Soedinenii 9, 722 (1973); Chem. Abs. 81, 136018 (1974).

    Google Scholar 

  13. Abyshev, A. Z., and P. P. Denisenko: Partial Synthesis of (±)-Pranferol. Khim. prirod. Soedinenii 7, 522 (1971); Chem. Abs. 75, 140731 (1971).

    Google Scholar 

  14. Abyshev, A. Z., and P. P. Denisenko: The Structure of Prangeferol: Khim. prirod. Soedinenii 8, 114 (1972); Chem. Abs. 77, 88220 (1972).

    Google Scholar 

  15. Abyshev, A. Z., P. P. Denisenko, N. P. Kostyuchenko, O. S. Anisimova, A. I. Ermakov, and Y. N. Sheinker: Pranferin, a New Coumarin from the Roots of Prangos ferulacea. Khim. prirod. Soedinenii 6, 675 (1970); Chem. Abs. 74, 111860 (1971).

    Google Scholar 

  16. Abyshev, A. Z., P. P. Denisenko, N. P. Kostyuchenko, A. I. Ermakov, and Y. N., Sheinker: Gosferol, a New Furocoumarin from the Roots of Prangos ferulacea. Khim. prirod. Soedinenii 8, 49 (1972); Chem. Abs. 77, 58792 (1972).

    Google Scholar 

  17. Abyshev, A. Z., P. P. Denisenko, N. P. Kostyuchenko, A. I. Ermakov, and Y. N., Sheinker: Natural Acetate of Meranzin Hydrate, a New Component of the Roots of Prangos ferulacea. Khim. prirod. Soedinenii 8, 608 (1972); Chem. Abs. 78, 121365 (1973).

    Google Scholar 

  18. Abyshev, A. Z., and A. M. Kutnevich: A Study of the Coumarin Composition of the Roots of Prangos uloptera. Khim. prirod. Soedinenii 4, 378 (1968); Chem. Abs. 70, 84948 (1969).

    Google Scholar 

  19. Abyshev, A. Z., A. M. Kutnevich, N. P. Kostyuchenko, O. A. Anisimova, A. I. Ermakov, and Y. N. Sheinker: The Structure of Ulopterol. Khim. prirod. Soedinenii 6, 300 (1970); Chem. Abs. 73, 76997 (1970).

    Google Scholar 

  20. Ahluwalia, V. K., V. N. Gupta, C. L. Rustagi, and T. R. Seshadri: Partial Methyl

    Google Scholar 

  21. Naturally Occurring Plant Coumarins Ethers of Polyhydroxy Coumarins: Synthesis of Isofraxidin and Fraxetin and Ring Isomeric Change in Coumarins. J. Sci. Ind. Res., India 19B, 345 (1960).

    Google Scholar 

  22. Ahluwalia, V. K., T. R. Seshadri, and P. Venkateswarlu: A Convenient Synthesis of Bergapten. Indian J. Chem. 7, 831 (1969).

    CAS  Google Scholar 

  23. Ahluwalia, V. K., T. R. Seshadri, and P. Venkateswarlu: A Total Synthesis of Isopimpinellin. Indian J. Chem. 9, 194 (1971).

    CAS  Google Scholar 

  24. Akramov, S. T., K. S. Mukhamedova, M. R. Yagudaev, and S. Y. Yunosov: NMR Spectrum of Prangosine. Khim. prirod. Soedinenii 3, 287 (1967); Chem. Abs. 67, 116998 (1967).

    Google Scholar 

  25. Aminov, A. M., K. B. Bizhanova, and G. K. Nikonov: Coumarins of Libanotis lehmanniana. Khim. prirod. Soedinenii 11, 246 (1975); Chem. Abs. 83, 144484 (1975).

    Google Scholar 

  26. Aminov, A. M., and G. K. Nikonov: Coumarins of Seseli tenuisectum. Khim. prirod. Soedinenii 8, 38 (1972); Chem. Abs. 77, 58793 (1972).

    Google Scholar 

  27. A Study of the Components of the Roots of Seseli tschuense. Khim. prirod. Soedinenii 8, 799 (1972); Chem. Abs. 78, 108204 (1973).

    Google Scholar 

  28. The Structure of Chuin, a New Coumarin from the Roots of Seseli tschuense. Khim. prirod. Soedinenii 9, 487 (1973); Chem. Abs. 80, 105843 (1974).

    Google Scholar 

  29. Structure of the Coumarin, Sechulin. Khim. prirod. Soedinenii 10, 152 (1974); Chem. Abs. 81, 105334 (1974).

    Google Scholar 

  30. Andrianova, V. B., and Y. E. Sklyar: Isopeucenidin from Libanotis montana. Khim. prirod. Soednineii 11, 89 (1975); Chem. Abs. 83, 128636 (1975).

    Google Scholar 

  31. Andrianova, V. B., Y. E. Sklyar, M. E. Perel’son, and M. G. Pimenov: Kellerin, a New Coumarin from the Roots of Ferula kelleri. Khim. prirod. Soedinenii 9, 795 (1973); Chem. Abs. 81, 120383 (1974).

    Google Scholar 

  32. Aplin, R. T., and C. B. Page: The Constituents of Native Umbelliferae, Part 1. Coumarins from Dill (Anetheum graveolens L.). J. Chem. Soc. (C) 1967, 2593.

    Google Scholar 

  33. Artem’eva, M. V., M. O. Karryev, and G. K. Nikonov: Isofraxetin, a New Coumarin Extracted from Fraxinus potamophila. Izvest. Akad. Nauk Turkm. S.S.R., Ser. Biol. Nauk 1973, 63; Chem. Abs. 79, 89463 (1973).

    Google Scholar 

  34. Fraxinoside, a New Glucoside from Fraxinus potamophila. Izvest. Akad. Nauk Turkm. S.S.R., Ser. Biol. Nauk 1973, 82; Chem. Abs. 79, 146800 (1973).

    Google Scholar 

    Google Scholar 

  35. Artem’eva, M. V., G. K. Nikonov, and M. O. Karryev: Coumarins of Fraxinus mandschurica and F. potamophila. Khim. prirod. Soedinenii 9, 493 (1973); Chem. Abs. 80, 105844 (1974).

    Google Scholar 

  36. Arthur, H. C., and C. M. Lee: An Examination of the Rutaceae of Hong Kong. Part V. A New Coumarin, Avicennin, from the Bark of Zanthoxylum avicennae. J. Chem. Soc. 1960, 4654.

    Google Scholar 

  37. Arthur, H. C., and W. D. Ollis: A Revised Structure for Avicennin. J. Chem. Soc. 1963, 3910.

    Google Scholar 

  38. Atkinson, E., D. R. Boyd, and M. F. Grundon: Coumarins of Skimmia japonica. Phytochemistry 13, 853 (1974).

    CAS  Google Scholar 

  39. Austin, P. W., and T. R. Seshadri: Synthesis of Naturally Occurring Coumarin Derivatives: Part I — Synthesis of Dihydroseselin, Dihydroxanthyletin, Demethyl- suberosin and Suberosin. Indian J. Chem. 6, 412 (1968).

    CAS  Google Scholar 

  40. Austin, P. W., T. R. Seshadri, M. S. Sood, and Vishwapaul: Components of Seseli sibiricum. Constitution and Synthesis of Sibiricin, a New Coumarin. Tetrahedron 24, 3247 (1968).

    CAS  Google Scholar 

  41. Avramenko, L. G., and G. K. Nikonov: Saxalin, a New Furocoumarin from the Roots of Angelica saxatilis. Khim. prirod. Soedinenii 7, 830 (1971); Chem. Abs. 76, 138170 (1972).

    Google Scholar 

  42. Avramenko, L. G., G. K. Nikonov, and M. G. Pimenov: Andelin, a New Dihydropyranocoumarin from the Root of Angelica decursiva. Khim. prirod. Soedinenii 6, 190 (1970); Chem. Abs. 73, 87814 (1970).

    Google Scholar 

  43. Bagirov, V. Y., and N. P. Kir’yalov: Coumarins from the Roots of Ferula nevskii. Khim. prirod. Soedinenii 6,465 (1970); Chem. Abs. 74, 11044 (1971).

    Google Scholar 

  44. Bagirov, V. Y., and N. P. Kir’yalov: A Coumarin from the Roots of Ferula nevskii. Khim. prirod. Soedinenii 8, 387 (1972); Chem. Abs. 77, 139729 (1972).

    Google Scholar 

  45. Bagirov, V. Y., N. P. Kir’yalov, and V. I. Sheichenko: The Coumarin Tavicone from the Roots of Ferula karatavica. Khim. prirod. Soedinenii 5, 591 (1969); Chem. Abs. 73, 25241 (1970).

    Google Scholar 

  46. Structure of Samarcandin. Khim. prirod. Soedinenii 6, 465 (1970); Chem. Abs. 74, 8196 (1971).

    Google Scholar 

  47. Bagirov, V. Y., N. P. Kir’yalov, V. I. Sheichenko, and V. V. Bochkarov: Structure of Badrakemin. Khim. prirod. Soedinenii 6, 466 (1970); Chem. Abs. 73, 124595 (1970).

    Google Scholar 

  48. Bagirov, V. Y., and V. I. Sheichenko: The Structure of Karatavic Acid. Khim. prirod. Soedinenii 11, 700 (1975); Chem. Abs. 84, 164564 (1976).

    Google Scholar 

  49. Bagirov, V. Y., and V. I. Sheichenko: The Structure and Stereochemistry of Tavicone: Khim. prirod. Soedinenii 12, 452 (1976); Chem. Abs. 85, 192493 (1976).

    Google Scholar 

  50. Bagirov, V. Y., V. I. Shhchenko, and A. I. Ban’kovskii: Stereochemistry of Nevskin. Khim. prirod. Soedinenii 12, 450 (1976).

    Google Scholar 

  51. Ballantyne, M. M., P. H. McCabe, and R. D. H. Murray: Claisen Rearrangements - II Synthesis of Six Natural Coumarins. Tetrahedron 27, 871 (1971).

    CAS  Google Scholar 

  52. Ballantyne, M. M., R. D. H. Murray, and A. B. Penrose: An Out-of-Ring Claisen Rearrangement During the Synthesis of Nieshoutin and Obliquetin. Tetrahedron Letters 1968, 4155.

    Google Scholar 

  53. Bandopadhyay, M., S. B. Malik, and T. R. Seshadri: Synthesis of New Cou­marin Components of Heracleum candicans. Indian J. Chem. 11, 530 (1973).

    CAS  Google Scholar 

  54. Bandopadhyay, M., N. P. Pardeshi, and T. R. Seshadri: Synthesis of Some Naturally Occurring Coumarins. Indian J. Chem. 12, 23 (1974).

    CAS  Google Scholar 

  55. Bandopadhyay, M., and T. R. Seshadri: Components of Heracleum candicans: Part I. Indian J. Chem. 8, 855 (1970).

    CAS  Google Scholar 

  56. Components of Heracleum candicans: Part II. Indian J. Chem. 8, 1146 (1970).

    Google Scholar 

  57. Ban’kovskii, A. I., N. E. Ermatov, and M. E. Perel’son: Libanoridin, a New Coumarin from Libanotis schrenkiana. Khim. prirod. Soedinenii 5, 52 (1969); Chem. Abs. 71, 7705 (1969).

    Google Scholar 

  58. Ban’kovskii, A. I., N. E. Ermatov, M. E. Perel’son, L. Bubeva-Ivanova, and N. S. Pavlova: Structure of the Coumarins Colladin and Colladonin. Khim. prirod. Soedinenii 6, 173 (1970); Chem. Abs. 73, 76988 (1970).

    Google Scholar 

  59. Barnes, C. S., and J. L. Occolowitz: The Mass Spectra of Some Naturally Occurring Oxygen Heterocycles and Related Compounds. Austral. J. Chem. 17, 975 (1964).

    CAS  Google Scholar 

  60. Basa, S. C.: Crenulatin, a Formyl Coumarin from Hesperathusa crenulata (Rutaceae). Austral. J. Chem. 28, 1159 (1975).

    CAS  Google Scholar 

  61. Basa, S. C, J. Chatterjee, and A. Chatterjee: Extractives of Umbelliferae: Pabularirone, a New Furocoumarin from Prangos pabularia Lindl. Chem. and Ind. 1970, 746.

    Google Scholar 

  62. Basa, S. C, J. Chatterjee, and A. Chatterjee: Pabulenol — a Biological Transformation Product of Oxypeucedanin. Tetrahedron Letters 1971, 1977.

    Google Scholar 

  63. Bates, R. B., D. J. Eckert, S. K. Paknikar, and V. P. Thalacker: Structure and Synthesis of Archangelin. Spectral Methods for Distinguishing Bergaptyl from Isobergaptyl Ethers. Tetrahedron Letters 1972, 3811.

    Google Scholar 

  64. Bates, R. B., J. H. Schäuble, and M. Soucek: The CioHn Side Chain in Mycelian- amide. The Stereochemistry of Bergamottin and Umbelliprenin. Tetrahedron Letters 1963, 1683.

    Google Scholar 

  65. Begley, M. J., L. Crombie, D. A. Slack, and D. A. Whiting: Course of the Condensation between 5,7-Dihydroxycoumarin and Citral: A Reinvestigation of the Constitution of Bruceol and Deoxybruceol from Eriostemon brucei. J. C. S. Chem. Comm. 1976, 140.

    Google Scholar 

  66. Bencze, W., J. Eisenbeiss, and H. Schmid: Die Konstitution des Visamminols. Helv. Chim. Acta 39, 923 (1956).

    CAS  Google Scholar 

  67. Bernotat-Wulf, H., A. Niggli, L. Ulrich, and H. Schmid: Über die absolute Konfiguration der Visnagane. Helv. Chim. Acta 52, 1165 (1969).

    CAS  Google Scholar 

  68. Bevan, C. W. L., and D. E. U. Ekong: Occurrence of 8-Methoxy-4-methyl-coumarin in Ekebergia senegalensis. A. Juss. Chem. and Ind. 1965, 383.

    Google Scholar 

  69. Bhanu, S., T. Saroja, T. R. Seshadri, and S. K. Mukerjee: A Synthesis of Halfordin. Indian J. Chem. 9, 380 (1971).

    CAS  Google Scholar 

  70. Bhanu, S., T. Saroja, T. R. Seshadri, and S. K. Mukerjee: New Syntheses of Halkendin and Isohalkendin. Indian J. Chem. 10, 16 (1972).

    CAS  Google Scholar 

  71. Bhardwaj, D. K., R. Murari, T. R. Seshadri, and R. Singh: Liqcoumarin, a Novel Coumarin from Glycyrrhiza glabra. Phytochemistry 15, 1182 (1976).

    CAS  Google Scholar 

  72. Bhardwaj, D. K., R. Murari, T. R. Seshadri, and R. Singh: Lacoumarin from Lawsonia inermis. Phytochemistry 15, 1789 (1976).

    CAS  Google Scholar 

  73. Birch, A. J., M. Maung, and A. Pelter: Studies in Relation to Biosynthesis XL. Some Aspects of the Chemistry of o-Isopentenylphenols and Related Compounds. Austral. J. Chem. 22, 1923 (1969).

    CAS  Google Scholar 

  74. Bohlmann, F., V. S. Bhaskar Rao, and M. Grenz: Über die Cumarine aus Angelica ursina und Seseli libanotis. Tetrahedron Letters 1968, 3947.

    Google Scholar 

  75. Bohlmann, F., and E. Clausen: Natürlich vorkommende Cumarin-Derivate, VI. Über die Inhaltsstoffe von Capnophyllum-Arten. Chem. Ber. 103, 3619 (1970).

    CAS  Google Scholar 

  76. Bohlmann, F., and H. Franke: Natürlich vorkommende Cumarin-Derivate, VII. Synthese von racemischen Lomatin, Columbianetin, Angenomalin und Samidin. Chem. Ber. 104, 3229 (1971).

    CAS  Google Scholar 

  77. Bohlmann, F., and H. Franke: Isolation of obliquin from Phaenocoma prolifera. Phytochemistry 12, 726 (1973).

    CAS  Google Scholar 

  78. Bohlmann, F., H. Franke, and C. Zdero: Natürlich vorkommende Cumarin- Derivate, VIII. Struktur und Synthese eines neuen Cumarins aus Choisya ternata Kunth. Anales de Quirn 68, 765 (1972).

    Google Scholar 

  79. Bohlmann, F., and M. Grenz: Natürlich vorkommende Cumarine-Derivate. IV. Über neue Furocoumarine aus Ligusticum pyrenaicum Koch. Chem. Ber. 102, 1673 (1969).

    CAS  Google Scholar 

  80. Bohlmann, F., and M. Grenz: Natürlich vorkommende Cumarine-Derivate, X. Notiz über die Inhaltsstoffe von Cnidium silaifolium (Jacq.). Sim. Chem. Ber. 106, 1047 (1973).

    CAS  Google Scholar 

  81. Bohlmann, F., and M. Grenz: Natürlich vorkommende Cumarine-Derivate, XI. Über die Inhaltsstoffe von Gerbera piloselloides Cass. Chem. Ber. 108, 26 (1975).

    CAS  Google Scholar 

  82. Bohlmann, F., and M. Grenz: Natürlich vorkommende Cumarine-Derivate, XIII. Notiz über zwei neue Cumarine-Derivate aus Machaeranthera scabrella (Greene) Shinners. Chem. Ber. 109, 1584 (1976).

    CAS  Google Scholar 

  83. Bohlmann, F., M. Grenz, and C. Zdero: Natürlich vorkommende Cumarine- Derivate, XII. Neue Cumarine aus Peucedanum- und Pteronia-Arten. Chem. Ber. 108, 2955 (1975).

    CAS  Google Scholar 

  84. Bohlmann, F., J. Jacob, and M. Grenz: Natürlich vorkommende Terpen-Derivate, XLV. Über Inhaltsstoffe von Scaevola lobelia (Th.) Murr. Chem. Ber. 108, 433 (1975).

    CAS  Google Scholar 

  85. Bohlmann, F., and D. Körnig: Natürlich vorkommende Terpen-Derivate, XXXVIII. Synthese von Cumarine-Terpenen. Chem. Ber. 107, 1780 (1974).

    CAS  Google Scholar 

  86. Bohlmann, F., and K. M. Rode: Natürlich vorkommende Cumarine-Derivate, II. Über die Cumarine aus Libanotis buchtormensis. Chem. Ber. 101, 2741 (1968).

    CAS  Google Scholar 

  87. Bohlmann, F., D. Schumann, and C. Zdero: Natürlich vorkommende Terpen- Derivate, XXVIII. Über ein neues Sesquiterpen-Derivate aus Artemisia pontica L. Chem. Ber. 107, 644 (1974).

    CAS  Google Scholar 

  88. Bohlmann, F., and W. Thefeld: Natürlich vorkommende Cumarine-Derivate, V. Neue Dihydroseselin-Derivate aus Laserpitium archangelica Wulf (1). Tetrahedron Letters 1970, 3577.

    Google Scholar 

  89. Bohlmann, F., and C. Zdero: Natürlich vorkommende Terpen-Derivate, XLVIII. Über neue Inhaltsstoffe der Gattung Anthemis. Chem. Ber. 108, 1902 (1975).

    CAS  Google Scholar 

  90. Bohlmann, F., C. Zdero, and H. Franke: Natürlich vorkommende Cumarine- Derivate, IX. Über die Inhaltsstoffe der Gattung Gerbera. Chem. Ber. 106, 382 (1973).

    CAS  Google Scholar 

  91. Bohlmann, F., C. Zdero, and H. Kapteyn: Über Cumarine-Derivate aus Pflanzen der Gattung Aster. Annalen 717, 186 (1968).

    CAS  Google Scholar 

  92. Böhm, B. A., R. K. Ibrahim, and G. H. N. Towers: The Partial Elucidation of the Structure of a New Coumarin from Hydrangea macrophylla. Canad. J. Biochem. Physiol. 39, 1389 (1961).

    Google Scholar 

  93. Borisov, V. N., A. I. Ban’kovskii, N. S. Pavlova, L. Bubeva-Ivanova. V. I. Sheichenko, and V. S. Kabanov: Colladocin, a New Terpenoid Coumarin from Colla- donia triquetra. Khim. prirod. Soedinenii 11, 247 (1975); Chem. Abs. 83, 59096 (1975).

    Google Scholar 

  94. Borisov, V. N., A. I. Ban’kovskii, V. I. Sheichenko, and V. S. Kabanov: Iso- samarcandin from Ferula microloba. Khim. prirod. Soedinenii 10, 786 (1974); Chem. Abs. 82, 135686 (1975).

    Google Scholar 

  95. Borisov, V. N., A. I. Ban’kovskii, V. I. Sheichenko, V. S. Kabanov, and P. I. Zakharov: Methyl Galbanate — New Terpenoid Coumarin from Ferula microloba. Khim. prirod. Soedinenii 10, 516 (1974); Chem. Abs. 82, 14007 (1975).

    Google Scholar 

  96. Borisov, V. N., A. I. Ban’kovskii, V. I. Sheichenko, and M. G. Pimenov: Coumarins of Ferula tuberifera. Khim. prirod. Soedinenii 10, 515 (1974); Chem. Abs. 82, 28588 (1975).

    Google Scholar 

  97. Borisov, V. N., A. I. Ban’kovskii, V. I. Sheichenko, M. G. Pimenov, and P. I. Zakharov: The Structure of Galbanic Acid. Khim. prirod. Soedinenii 9, 429 (1973); Chem. Abs. 79, 91913 (1973).

    Google Scholar 

  98. Bottomley, W.: Discophoridin, a New Coumarin from Velleia discophora F. Muell. Austral. J. Chem. 16, 143 (1963).

    CAS  Google Scholar 

  99. Braga de Oliveira, A., L. G. Fonseca e Silva, and O. R. Gottlieb: Flavonoids and Coumarins from Platymiscium praecox. Phytochemistry 11, 3515 (1972).

    Google Scholar 

  100. Braz Filho, R., A. F. Magalhaes, and O. R. Gottlieb: A Quimica de Moräceas Brasileiras I. Novas Cumarinas do Brosimum paraense. Anais Acad, brasil Cienc. 42, 139 (1970); Chem. Abs. 75, 724586 (1971).

    Google Scholar 

  101. Braz Filho, R., A. F. Magalhaes, and O. R. Gottlieb: Chemistry of Brazilian Moraceae II. Brosiparin and Other Coumarins from Brosimum rubescens. Anais Acad, brasil Cienc. 43, 585 (1971); Chem. Abs. 77, 161990 (1972).

    Google Scholar 

  102. Braz Filho, R., A. F. Magalhaes, and O. R. Gottlieb: Coumarins from Brosimum rubescens. Phytochemistry 11, 3307 (1972).

    CAS  Google Scholar 

  103. Brooker, R. M., J. N. Eble, and N. A. Starkowsky: Chalepensin, Chalepin and Chalepin Acetate, Three Novel Furocoumarins from Rut a chalepensis. Lloydia 30, 73 (1967).

    CAS  Google Scholar 

  104. Brown, D., R. O. Asplund, and V. A. McMahon: An NMR Procedure for Determining Methoxy Positions of Coumarin Trimethyl Ethers using the Benzene In­duced Solvent Shift. Phytochemistry 13, 1923 (1974).

    CAS  Google Scholar 

  105. Brown, D., R. O. Asplund, and V. A. McMahon: Phenolic Constituents of Artemisia tridentata spp. vaseyana. Phytochemistry 14, 1083 (1975).

    CAS  Google Scholar 

  106. Brown, S. A.: Recent Studies on the Formation of Natural Coumarins. Lloydia 26, 211 (1963).

    CAS  Google Scholar 

  107. Brown, S. A., M. El-Dakhakhny, and W. Steck: Biosynthesis of Linear Furano- coumarins. Canad. J. Biochem. 48, 863 (1970).

    CAS  Google Scholar 

  108. Brown, S. A., and W. Steck: 7-Demethylsuberosin and Osthenol as Intermediates in Furanocoumarin Biosynthesis. Phytochemistry 12, 1315 (1973).

    CAS  Google Scholar 

  109. Brown, S. A., G. H. N. Towers, and D. Chen: Biosynthesis of the Coumarins-V. Pathways of Umbelliferone Formation in Hydrangea macrophylla. Phytochemistry 3, 469 (1964).

    CAS  Google Scholar 

  110. Bubeva-Ivanova, L., and N. S. Pavlova: Phytochemical Study of Colladonia triquetra. I. Natural Coumarins. Farmatsiya (Bulgaria) 1, 30 (1969); Chem. Abs. 71, 57558 (1969).

    Google Scholar 

  111. Budzikiewicz, H., C. Djerassi, and D. H. Williams: Structure Elucidation of Natural Products by Mass Spectrometry. 2. San Francisco: Holden-Day. 1964.

    Google Scholar 

  112. Caglioti, L., H. Naef, D. Arigoni, and O. Jeger: Zur Kenntnis der Sesquiterpene und Azulene. Über die Inhaltsstoffe der Asa foetida I. Farnesiferol A. Helv. Chim. Acta 41, 2278 (1958).

    CAS  Google Scholar 

  113. Caglioti, L., H. Naef, D. Arigoni, and O. Jeger: Zur Kenntnis der Sesquiterpene und Azulene. Über die Inhaltsstoffe der Asa foetida II. Farnesiferol B und C. Helv. Chim. Acta 42, 2557 (1959).

    CAS  Google Scholar 

  114. Call, T. G.: Extractive Studies and the Volatile Oil from the Fruits of Lomatium suksdorfii. Proc. Montana Acad. Sci. 17, 37 (1957); Chem. Abs. 52, 4102 (1958).

    Google Scholar 

  115. Call, T. G., and E. B. Fischer: Some Pharmacological Effects of the Roots of Pteryxia terebinthina var. terebinthina, and of Pteryxin, a Substance Isolated from the Roots. Northwest Sci. 32, 96 (1958); Chem. Abs. 53, 6429 (1959).

    Google Scholar 

  116. Cannava, A.: Is 3-Methyl-4-hydroxycoumarin the Active Substance Responsible for the Hypoprothrombinemia Produced by Ferula communisl Boll. chim. Farm. 97, 207 (1958); Chem. Abs. 52, 18689 (1960).

    Google Scholar 

  117. Caporale, G., and G. Rodighiero: Furocoumarins in the Roots of Angelica sylvestris. Ricerca Sci., Rend. Sec. B 1, 127 (1961); Chem. Abs. 57, 2596 (1962).

    Google Scholar 

  118. Carboni, S., V. Malaguzzi, and A. Marsili: Ferulenol, a New Coumarin Derivative from Ferula communis. Tetrahedron Letters 1964, 2783.

    Google Scholar 

  119. Cardillo, G., R. Cricchio, L. Merlini, and G. Nasini: Poliisoprenifoli naturali. Sintesi della grifolina e della ostrutina. Gazzetta 99, 308 (1969).

    CAS  Google Scholar 

  120. Carman, R. M., F. N. Lahey, and J. K. McLeod: Geiparvarin: Proton Magnetic Resonance Studies. Austral. J. Chem. 20, 1957 (1967).

    CAS  Google Scholar 

  121. Carpenter, I., E. J. McGarry, and F. Scheinmann: The Neoflavonoids and 4-Alkylcoumarins from Mammea africana G. Don. Tetrahedron Letters, 1970, 3983.

    Google Scholar 

  122. Carpenter, I., E. J. McGarry, and F. Scheinmann: Extractives from Guttiferae. Part XXI. The Isolation and Structure of Nine Coumarins from the Bark of Mammea africana G. Don. J. Chem. Soc. (C) 1971, 3783.

    Google Scholar 

  123. Cave, A., M. Debray, G. Henry, J. Kunesch, and J. Polonsky: Sur la structure d’une nouvelle alkyl-4 coumarine isolée de Calophyllum inophyllum. Compt. rend. 275, C, 1105 (1972).

    Google Scholar 

  124. Chakraborty, D. P., B. K. Chowdhury, and B. C. Das: Mexoticin, a New Cou­marin from Murraya exotica L. (1). Tetrahedron Letters 1967, 3471.

    Google Scholar 

  125. Chang, P. T. O., G. A. Cordell, G. H. Aynilian, H. H. S. Fong, and N. R. Farnsworth: Alkaloids and Coumarins of Thamnosma montana. Lloydia 39, 134 (1976).

    CAS  Google Scholar 

  126. Chatterjee, A., J. Banerji, and S. C. Basa: Lactonic Constituents of Prangos pabularia Lindl (Umbelliferae). Tetrahedron 28, 5175 (1972).

    CAS  Google Scholar 

  127. Chatterjee, A., and A. Bhattacharya: The Isolation and Constitution of Marmin, a New Coumarin from Aegle marmelos Correa. J. Chem. Soc. 1959, 1922.

    Google Scholar 

  128. Chatterjee, A., P. K. Bose, and S. K. Saha: Ferulin, the Main Lactone of Ferula alliacea. Arch. Pharm. 295, 248 (1962).

    CAS  Google Scholar 

  129. Chatterjee, A., C. P. Dutta, and S. Bhattacharyya: Micromelumin and Micro- pubescin — Two New Coumarins from Micromelum pubescens L. (Fam. Rutaceae). Sci. Cult. 33, 371 (1967); Chem. Abs. 69, 2887 (1968).

    Google Scholar 

  130. Chatterjee, A., C. P. Dutta, and S. Bhattacharyya: Structure of Micropubescin, a New Coumarin from Micromelum pubescens. Sci. Cult. 34, 366 (1968); Chem. Abs. 70, 114946 (1969).

    Google Scholar 

  131. Chatterjee, A., C. P. Dutta, S. Bhattacharyya, H. E. Audier, and B. C. Das: The Structure of Marmin. Tetrahedron Letters 1967, 471.

    Google Scholar 

  132. Chatterjee, A., and S. Dutta: Structure Investigation of New Lactonic Constituents from the Roots of Angelica archangelica Linn. Indian J. Chem. 6, 415 (1968).

    CAS  Google Scholar 

  133. Chatterjee, A., R. N. Rej, A. Banerji, and J. Banerji: Abnormal Rearrangement of Isoprenoid Epoxide: Synthesis of 7-Methoxy-8-(2’-formyl-2’-methylpropyl)-couma- rin, the Lactonic Constituent of Grapefruit Peel Oil of Citrus decumana Linn. ( Rutaceae ). Chem. and Ind. 1976, 410.

    Google Scholar 

  134. Chatterjee, A., and S. Sen Gupta: The Constitution of Archangelin, a New Coumarin Isolated from the Root of Angelica archangelica Linn. ( Umbelliferae ). Tetrahedron Letters, 1964, 1961.

    Google Scholar 

  135. Chemical Section, Luminuous Fungus Co-Operative Research Group of Kiangsu: Armillariella tabescens. II. Isolation and Determination of the Structure of the Armillarisins. Wei Sheng Wu Hsueh Po 14, 9 (1974); Chem. Abs. 82, 40463 (1975).

    Google Scholar 

  136. Chernobai, V. T., and D. G. Kolesnikov: Coumarins of Cnidium dubium. Doklady Akad. Nauk S.S.S.R. 133, 233 (1960); Chem. Abs. 54, 23188 (1960).

    Google Scholar 

  137. Chexal, K. K., C. Fouweather, and J. S. E. Holker: Biosynthesis of Fungal Metabolites VII. Production and Biosynthesis of 4,7-Dimethoxy-5-methylcoumarin in Aspergillus variecolor. J. C. S. Perkin I 1975, 554.

    Google Scholar 

  138. Chi, H.-J.: Components of Umbelliferous Plants in Korea. IV. Coumarin Derivatives of the Root of Angelica. Yakhak Hoeji 11, 36 (1967); Chem. Abs. 71, 36408 (1969).

    Google Scholar 

  139. Chow, P. W., A. M. Duffield, and P. R. Jefferies: The Chemistry of the Western Australian Rutaceae V. The Isolation of Some Coumarins and the Structure of Phebalosin. Austral. J. Chem. 19, 483 (1966).

    CAS  Google Scholar 

  140. Coates, R. M., and L. S. Melvin: Total Synthesis of (±)-Marmin and Related Coumarin Monoterpenes. Tetrahedron 26, 5699 (1970).

    CAS  Google Scholar 

  141. Combes, G., R. Pernet, and R. Pierre: Sur l’isolement, la structure et les propriétés d’une nouvelle coumarine extraite de Toddalia aculeata Pers. Bull. Soc. chim. France 1961, 1609.

    Google Scholar 

  142. Cordova B, H. E., and L. N. Garelli M.: A New Coumarin in Amyris simpli- cifolia. Phytochemistry 13, 758 (1974).

    Google Scholar 

  143. Crombie, L., D. E. Games, N. J. Haskins, and G. F. Reed: Isolation and Structure of Insecticidal Components from Mammea americana L. Tetrahedron Letters 1970, 251.

    Google Scholar 

  144. Crombie, L., D. E. Games, N. J. Haskins, and G. F. Reed: Extractives of Mammea americana L. Part III. Identification of New Coumarin Relatives of Mammea B/BA, B/BB and B/BC having 5,6-Annulation and Higher Oxidation Levels. J. C. S. Perkin I 1972, 2241.

    Google Scholar 

  145. Crombie, L., D. E. Games, N. J. Haskins, and G. F. Reed: Extractives of Mammea americana L. Part IV. Identification of New 7,8- Annulated Relatives of the Coumarins Mammea A/A A, A/AB, B/AA, and B/AB, and New Members of the 6-Acyl Family B/AA, B/AB, and B/AC. J. C. S. Perkin I 1972, 2248.

    Google Scholar 

  146. Crombie, L., D. E. Games, N. J. Haskins, and G. F. Reed: Extractives of Mammea americana L. Part V. The Insecticidal Compounds. J. C. S. Perkin I 1972, 2255.

    Google Scholar 

  147. Crombie, L., D. E. Games, N. J. Haskins, G. F. Reed, R. A. Finnegan, and K. E. Merkel: Identification of Nine New 5,6-Annulated Relatives of the Mammea coumarins B/BA, B/BB, and B/BC. Tetrahedron Letters 1970, 3975.

    Google Scholar 

  148. Crombie, L., D. E. Games, N. J. Haskins, G. F. Reed, R. A. Finnegan, and K. E. Merkel: Identification of New Mammea Coumarins: Four 7,8-Annulated Relatives of the Mammea Coumarins A/AA-A/AB, B/AA, B/AB, and Two of the 6-Acyl Family B/AA ( Isomammein) and B/AB. Tetrahedron Letters 1970, 3979.

    Google Scholar 

  149. Crombie, L., D. E. Games, and A. McCormick: Isolation and Structure of Mammea B/BA, B/BB, B/BC and C/BB: A Group of 4-n-Propyl- and 4-n-Amyl-Coumarin Extractives of Mammea americana L. Tetrahedron Letters 1966, 151.

    Google Scholar 

  150. Crombie, L., D. E. Games, and A. McCormick: Extractives of Mammea americana L. Part I. The 4-n-Alkylcoumarins. Isolation and Structure of Mammea B/BA, B/BB, B/BC and C/BB. J. Chem. Soc. (C) 1967, 3545.

    Google Scholar 

  151. Crombie, L., and R. Ponsford: Pyridine-Catalyzed Condensation of Citral with Phloroglucinols, a Novel Reaction Leading to Tetracyclic Bis-Ethers and Chromenes. J. Chem. Soc. (C) 1971, 788.

    Google Scholar 

  152. Cussans, N. J., and T. N. Huckerby: Carbon-13 NMR Spectroscopy of Hetero­cyclic Compounds — IV. A 20 MHz Study of Chemical Shifts and Carbon-Proton Coupling Constants in a Series of Hydroxy, Methoxy and Glucosyl Coumarins. Tetra­hedron 31, 2719 (1975).

    CAS  Google Scholar 

  153. Dall’acqua, F., A. Capozzi, S. Marciani, and G. Caporale: Biosynthesis of Furocoumarins: Further Studies on Ruta graveolens. Z. Naturforsch. 27b, 813 (1972).

    Google Scholar 

  154. Dean, F. M.: Naturally Occurring Coumarins;. Fortschr. Chem. org. Naturstoffe 9, 225 (1952).

    CAS  Google Scholar 

  155. Dean, F. M.: In: Naturally Occurring Oxygen Ring Compounds. London: Butterworths. 1963.

    Google Scholar 

  156. Dean, F. M., and B. Parton: The Structure and Synthesis of (+)-Obliquin. J. Chem. Soc. (C) 1969, 526.

    Google Scholar 

  157. Dean, F. M., B. Parton, N. Somvichien, and D. A. H. Taylor: The Coumarins of Ptaeroxylon obliquum. Tetrahedron Letters 1967, 2147.

    Google Scholar 

  158. Dean, F. M., and D. A. H. Taylor: Extractives from East African Timbers. Part II. Ptaeroxylon obliquum. J. Chem. Soc. (C) 1966, 114.

    Google Scholar 

  159. Delle Monache, F., F. Marletti, and G. Marini-Bettolo: Coumarins of Hortia arborea (Rutaceae): Hortiline and Hortiolone. Gazzetta 106, 681 (1976).

    CAS  Google Scholar 

  160. Deshmukh, M. N., V. H. Deshpande, and A. V. R. Rao: Two New Coumarins from Toddalia aculeata. Phytochemistry 15, 1419 (1976).

    CAS  Google Scholar 

  161. Djerassi, C., E. J. Eisenbraun, R. A. Finnegan, and B. Gilbert: Naturally Occurring Oxygen Heterocyclics. V. Mammein. Tetrahedron Letters 1959, 10.

    Google Scholar 

  162. Djerassi, C., E. J. Eisenbraun, R. A. Finnegan, and B. Gilbert: Naturally Occurring Oxygen Heterocyclics VII. The Structure of Mammein. J. Org. Chem. 25, 2164 (1960).

    CAS  Google Scholar 

  163. Djerassi, C., E. J. Eisenbraun, B. Gilbert, A. J. Lemin, S. P. Marfey, and M. P. Morris: Naturally Occurring Oxygen Heterocyclics. II. Characterisation of an Insecticidal Principle from Mammea americana L. J. Amer. Chem. Soc. 80, 3686 (1958).

    CAS  Google Scholar 

  164. Dreyer, D. L.: Constituents of Thamnosma montana Torr. and Frem. Tetrahedron 22, 2923 (1966).

    CAS  Google Scholar 

  165. Dreyer, D. L.: Chemotaxonomy of the Rutaceae — II. Extractives of Severinia buxifolia (Poir.) Ten. Tetrahedron 23, 4613 (1967).

    CAS  Google Scholar 

  166. Dreyer, D. L.: Chemotaxonomy of the Rutaceae. IV. Constituents of Murraya paniculata (Linn.) Jack. J. Org. Chem. 33, 3574 (1968).

    CAS  Google Scholar 

  167. Dreyer, D. L.: Coumarins and Alkaloids of the Genus Ptelea. Phytochemistry 8, 1013 (1969).

    CAS  Google Scholar 

  168. Dreyer, D. L.: Extractives of Angelica genuflexa Nutt. J. Org. Chem. 35, 2294 (1970).

    CAS  Google Scholar 

  169. Dreyer, D. L., and P. F. Huey: Coumarins of Citrus macroptera. Phytochemistry 12, 3011 (1973).

    CAS  Google Scholar 

  170. Dreyer, D. L., and A. Lee: Extractives of Geijera parviflora. Phytochemistry 11, 763 (1972).

    CAS  Google Scholar 

  171. Dreyer, D. L., K. P. Muderloh, and W. E. Thiessen: Extractives of Dalea Species (Leguminosae). Tetrahedron 31, 287 (1975).

    CAS  Google Scholar 

  172. Dreyer, D. L., M. V. Pickering, and P. Cohan: Distribution of Limonoids in the Rutaceae. Phytochemistry 11, 705 (1972).

    CAS  Google Scholar 

  173. Duffield, A. M., P. R. Jefferies, E. N. Maslen, and A. I. M. Rae: The Structure of Bruceol. Tetrahedron 19, 593 (1963).

    CAS  Google Scholar 

  174. Dukhovlinova, L. I., M. E. Perel’son, Y. E. Sklyar, and M. G. Pimenov: Coumarins of the Roots of Seseli iliense. Khim. prirod. Soedinenii 10, 308 (1974); Chem. Abs. 81, 105338 (1974).

    Google Scholar 

  175. Dukhovlinova, L. I., Y. E. Sklyar, and M. E. Perel’son: Secorin — A New Dihydrofurocoumarin from the Roots of Seseli coronatum. Khim. prirod. Soedinenii 9, 663 (1973).

    Google Scholar 

  176. Dukhovlinova, L. I., Y. E. Sklyar, and M. E. Perel’son: Coumarins of the Roots of Seseli coronatum. Khim. prirod. Soedinenii 10, 782 (1974); Chem. Abs. 82, 121668 (1975).

    Google Scholar 

  177. El-Antably, S. M., and T. O. Soine: Coumarins XII: Synthesis of (±)-cis-trans- 3’,4’-Dihydroxy-3’,4’-dihydroxanthyletin and Their Diesters. J. Pharm. Sci. 62, 1643 (1973).

    CAS  Google Scholar 

  178. El-Basyouni, S., and G. H. N. Towers: The Phenolic Acids in Wheat. Natural Occurrence of Orthoferulic Acid. Cañad. J. Biochem. 42, 493 (1964).

    CAS  Google Scholar 

  179. Ellis, B. E., and S. A. Brown: Isolation of Dimethylallylpyrophosphate: Umbelli- ferone Dimethylallyl Transferase from Ruta graveolens. Cañad. J. Biochem. 52, 734 (1974).

    CAS  Google Scholar 

  180. Ermatov, N. E., and A. I. Ban’kovskii: Chemical Study of Libanotis bucht or mensis. Trudy Vses. Nauch Issled. Inst. Lek. Aromat. Rast. 15, 149 (1969); Chem. Abs. 75, 16083 (1971).

    Google Scholar 

  181. Ermatov, N. E., A. I. Ban’kovskii, and M. E. Perel’son: Coumarins of Ferula penninervis. Khim. prirod. Soedinenii 2, 158 (1966); Chem. Abs. 65, 15790 (1966).

    Google Scholar 

  182. Ermatov, N. E., A. I. Ban’kovskii, and M. E. Perel’son: A New Coumarin from Libanotis schrenkiana. Khim. prirod. Soedinenii 5, 222 (1969); Chem. Abs. 72, 63616 (1970).

    Google Scholar 

  183. Ermatov, N. E., A. I. Ban’kovskii, M. E. Perel’son, G. P. Syrova, and Y. N. Sheinker: Coumarins of Libanotis buchtormensis. Khim. prirod. Soedinenii 4, 145 (1968); Chem. Abs. 70, 57702 (1969).

    Google Scholar 

  184. Ermatov, N. E., A. I. Ban’kovskii, M. E. Perel’son, G. P. Syrova, and Y. N. Sheinker: Structure of Kamolone and Kamolol, New Coumarins from Ferula penninervis. Khim. prirod. Soedinenii 5, 79 (1969); Chem. Abs. 71, 615712 (1969).

    Google Scholar 

  185. Eshiett, I. T., and D. A. H. Taylor: The Isolation and Structure Elucidation of Some Derivatives of Dimethylallyl-Coumarin, Chromone, Quinoline, and Phenol from Fagara Species and from Cedrelopsis grevei. J. Chem. Soc. (C), 1968, 481.

    Google Scholar 

  186. Ewing, J., G. K. Hughes, and E. Ritchie: The Chemical Constituents of Australian Zanthoxylum Species I. Suberosin, 6-(3,3-Dimethylallyl)-7-methoxycoumarin. Austral. J. Sci. Res. 3A, 342 (1950).

    Google Scholar 

  187. Fanghaenel, E., R. Tapanes, and J. P. Zayas: Analysis of the Coumarins of Centrifuged Essential Oils Produced in Cuba from the Lime (Citrus aurantifolia). Cienc. Fis. 3, 111 (1971); Chem. Abs. 78, 33779 (1973).

    Google Scholar 

  188. Finkelstein, N., and D. E. A. Rivett: Puberulin, a New Prenyloxy-Coumarin from Agathosma puberula. Phytochemistry 15, 1080 (1976).

    CAS  Google Scholar 

  189. Finnegan, R. A., B. Gilbert, E. J. Eisenbraun, and C. Djerassi: Naturally Occurring Oxygen Heterocyclics. VIII. Synthesis of Some Coumarins Related to Mammein. J. Org. Chem. 25, 2169 (1960).

    CAS  Google Scholar 

  190. Finnegan, R. A., and K. E. Merkel: Constituents of Mammea americana L. IX: Oxidation of Mammein and Mammeisin. J. Pharm. Sci. 61, 1603 (1972).

    CAS  Google Scholar 

  191. Finnegan, R. A., K. E. Merkel, and N. Back: Constituents of Mammea americana L. VIII: Novel Structural Variations on the Mammein Theme and Antitumor Activity of Mammein and Related Coumarin and Phloroglucinol Derivatives. J. Pharm. Sci. 61, 1599 (1972).

    CAS  Google Scholar 

  192. Fischer, F. C., P. H. Jasperse, J. Karlsen, and A. B. Svendsen: Ein neues Furanocoumaringlykosid aus Heracleum mantegazzianum. Phytochemistry 13, 2334 (1974).

    CAS  Google Scholar 

  193. Fischer, F. C, and A. B. Svendsen: Apterin, a Common Furanocoumarin Glycoside in the Umbelliferae. Phytochemistry 15, 1079 (1976).

    CAS  Google Scholar 

  194. Fish, F., A. 1. Gray, R. D. Waigh, and P. G. Waterman: Dipetalolactone: A Novel Pyranocoumarin from the Root Bark of Zanthoxylum dipetalum. Phyto- chemistry 15, 313 (1976).

    CAS  Google Scholar 

  195. Fish, F., A. I. Gray, and P. G. Waterman: Alkaloids, Coumarins, Triterpenes, and a Flavanone from the Root of Zanthoxylum dipetalum. Phytochemistry 14, 2073 (1975).

    CAS  Google Scholar 

  196. Fisher, J. F.. and H. E. Nordby: Isolation and Spectral Characterisation of Coumarins in Florida Grapefruit Peel Oil. J. Food Sci. 30, 869 (1965).

    CAS  Google Scholar 

  197. Two New Coumarins from Grapefruit Peel Oil. Tetrahedron 22, 1489 (1966).

    Google Scholar 

  198. Fisher, J. F., H. E. Nordby, A. C. Waiss, and W. L. Stanley: A New Coumarin from Grapefruit Peel Oil. Tetrahedron 23, 2523 (1967).

    CAS  Google Scholar 

  199. Floss, H. G.: Biosynthesis of Furanocoumarins. Recent Advan. Phytochem. 4, 143 (1972).

    CAS  Google Scholar 

  200. Floss, IT. G., and U. Mothes: On the Biosynthesis of Furocoumarins in Pimpinella magna. Phytochemistry 5, 161 (1966).

    CAS  Google Scholar 

  201. Fuhrer, H., T. R. Govindachari, B. S. Joshi, and B. R. Pai: Revised Structures of Clausenidin, Dentatin and the Identity of Dentatin with Poncitrin. Indian J. Chem. 8, 198 (1970).

    CAS  Google Scholar 

  202. Fujita, M., and T. Furuya: Pharmacognostic Study of Crude Drugs Containing Coumarins and Their Derivatives. II. On an Acylcoumarin Newly Isolated from Angelica Species in Japan. Yakugaku Zasshi 76, 538 (1956); Chem. Abs. 50, 13000 (1956).

    Google Scholar 

  203. Fukui, K., M. Nakayama, S. Fujimoto, and O. Fukuda: The Synthesis of Iso- halfordin. Experientia 25, 354 (1969).

    CAS  Google Scholar 

  204. Furuya, T., and H. Kojima: Gas-Liquid Chromatography of Coumarins. J. Chromat. 29, 382 (1967).

    CAS  Google Scholar 

  205. Games, D. E.: Identification of 4-Phenyl- and 4-Alkylcoumarins in Mammea ameri­cana L., Mammea africana G. Don and Calophyllum inophyllum by Gas Chromato- graphy-Mass Spectrometry. Tetrahedron Letters 1972, 3187.

    Google Scholar 

  206. Games, D. E., and N. J. Haskins: Synthesis of Some Dimethylpyrano- and 3-Methylbut-2-enyl-, -4-Phenyl- and -4-n-Propyl coumarins. J. Chem. Soc. (D) 1971, 1005.

    Google Scholar 

  207. Games, D. E., and A. H. Jackson: Identification of Naturally Occurring Plant Phenolics by Gas Chromatography — Mass Spectrometry. In: A. Frigerio (ed.) Proc. Int. Symp. Gas Chromat. Mass Spectrom., p. 261. Milan: Tamburini. 1972; Chem. Abs. 79, 2178 (1973).

    Google Scholar 

  208. Ganguly, A. K., B. S. Joshi, V. N. Kamat, and A. H. Manmade: Synthesis of Clau­senin, Xanthoxyletin, Alloxanthoxyletin, Xanthyletin and Nordalbergin. Tetrahedron 23, 4777 (1967).

    CAS  Google Scholar 

  209. Gashimov, N. F., and G. A. Kuznetsova: A New Coumarin, Obtusifol, from Haplophyllum obtusifolium. Khim. prirod. Soedinenii 10, 303 (1974); Chem. Abs. 81, 105411 (1974).

    Google Scholar 

  210. Gastaldi, C.: Active Principles in Ferula communis. Ricerca Sci. 28, 377 (1958); Chem. Abs. 52, 13011 (1960).

    Google Scholar 

  211. Ghosal, C. R., S. Sen Gupta, and A. Chatterjee: Prangolarine, the Optical Isomer of Oxypeucedanin, Isolated from the Roots of Prangos pabularia Lindl. ( Umbelliferae ). Chem. and Ind. 1963, 1430.

    Google Scholar 

  212. Giorgobiani, E. D., N. F. Komissarenko, and E. P. Kemertelidze: Biacangelicin and a New Natural Furocoumarin, Heracol, from the Fruit of Heracleum asperum. Soobshch. Akad. Nauk Gruz. S.S.R. 57, 97 (1970); Chem. Abs. 73, 38468 (1970).

    Google Scholar 

  213. González, A. G., J. T. Barroso, E. D. Chico, J. R. Luis, and F. R. Luís: Componentes de umbeliferas XI. Nueva cumarina del Heracleum pyrenaicum Lam. Anales de Quirn. 72, 584 (1976).

    Google Scholar 

  214. González, A. G., J. T. Barroso, J. R. Luis, and F. R. Luis: Componentes de um­belíferas III. Estructura de una nueva cumarina del Heracleum granatense Boiss. et Elench. Anales de Quím. 70, 369 (1974).

    Google Scholar 

  215. González, A. G., J. T. Barroso, J. R. Luis, and F. R. Luis: Componentes de umbelíferas VIL Dos nuevas cumarinas del Heracleum granatense Boiss. Elench. Anales de Quím. 70, 856 (1974).

    Google Scholar 

  216. González, A. G., J. L. Bretón, H. L. Dorta, M. A. M. Iniguez, and F. R. Luis: Aplicación de la resonancia magnética nuclear en el estudio de estructuras de cumarinas. Anales de Quim. 69, 1013 (1973).

    Google Scholar 

  217. González, A. G., R. J. Cardona, E. D. Chico, H. L. Dorta, and F. R. Luis: Com­ponentes de umbelíferas X. Cumarinas del Peucedanum bourgaei Lange in Wilk et Lange. Anales de Quím. 72, 568 (1976).

    Google Scholar 

  218. González, A. G., R. J. Cardona, H. L. Dorta, J. M. Medina, and F. R. Luis: Com­ponentes de umbelíferas XII. Dos nuevas cumarinas del Peucedanum stenocarpum Boiss. et Reuter. Anales de Quím. 72, 588 (1976).

    Google Scholar 

  219. González, A. G., R. J. Cardona, H. López, J. M. Medina, and F. R. Luis: Distri­bución de cumarinas en umbelíferas. Rev. Real Acad. Cieñe. Exact., Fis. Nat. 70, 109 (1976).

    Google Scholar 

  220. González, A. G., R. J. Cardona, J. M. Medina, and F. R. Luis: Componentes de umbelíferas VI. Cumarinas del Peucedanum officinale L. Anales de Quím. 72, 60 (1976).

    Google Scholar 

  221. Componentes de umbelíferas VIII. Dos nuevas cumarinas del Peucedanum stenocarpum Boiss. et Reuter. Anales de Quím. 72, 88 (1976).

    Google Scholar 

  222. González, A. G., R. J. Cardona, R. M. Ordonez, and F. R. Luis: Nuevas fuentes de cumarinas naturales XXV. Cumarinas del Haplophyllum hispanicum Spach. (H. linifolium L.). Anales de Quím. 69, 781 (1973).

    Google Scholar 

  223. González, A. G., E. D. Chico, H. L. Dorta, J. R. Luis, and F. R. Luis: Nuevas fuentes de cumarinas naturales XXX. Componentes químicos de las Ruta chalepensis y del Dictamnus hispanicus Webb. Anales de Quím. 73, 430 (1977).

    Google Scholar 

  224. González, A. G., E. D. Chico, H. L. Dorta, J. M. Medina, and F. R. Luis: Nuevas fuentes de cumarinas naturales XXIX. Tres nuevas cumarinas de una especie canaria de Ruta. Anales de Quím. 72, 191 (1976).

    Google Scholar 

  225. González, A. G., R. Estevez, J. B. Arencibia, and T. R. Perez: Nuevas fuentes de cumarinas naturales XXVI. Cumarins minoritarias de las hojas de la Ruta pinnata L. fil; sabandinol, nueva cumarina. Anales de Quim. 69, 1141 (1973).

    Google Scholar 

  226. González, A. G., R. Estevez, and I. Jaraíz: Nuevas fuentes de cumarinas naturales XVIII. Estructura de la sabandinona, nueva cumarina de los frutos de la Ruta pinnata L. fil. Anales de Quím. 66, 1017 (1970).

    Google Scholar 

  227. González, A. G., R. Estevez, and I. Jaraíz: Structure of Sabandinin and Other Coumarins Isolated from the Roots of Ruta pinnata. Phytochemistry 10, 1621 (1971).

    Google Scholar 

  228. González, A. G., R. Estevez, and I. Jaraíz: Pinnaterin, a New Coumarin from the Roots of Ruta pinnata. Phytochemistry 10, 1971 (1971).

    Google Scholar 

  229. González, A. G., R. Estevez, and I. Jaraíz: Nuevas fuentes de cumarinas naturales XXI. Sabandinona y tederina, nuevas cumarinas de los frutos de la Ruta pinnata L. fil. Anales de Quím. 68, 425 (1972).

    Google Scholar 

  230. González, A. G., B. M. Fraga, M. G. Hernández, and J. G. Luis: Siderin, a New Coumarin from Sideritis canadensis. Phytochemistry 11, 2115 (1972).

    Google Scholar 

  231. González, A. G., B. M. Fraga, M. G. Hernández, J. G. Luis, and W. Steck: Siderin: A Revised Structure. Chem. and Ind. 1974, 166.

    Google Scholar 

  232. González, A. G., B. M. Fraga, O. Pino, J. P. Declerq, G. Germain, and J. Fayos: X-Ray Structure of Bethancorol, a New Coumarin from Cneorum tricoccum. Tetra­hedron Letters 1976, 1729.

    Google Scholar 

  233. González, A. G., and F. R. Luis: Chemistry of the Rutaceae of the Canary Isles. Herba Hung. 10, 95 (1971); Chem. Abs. 79, 15854 (1973).

    Google Scholar 

  234. González, A. G., E. A. Martinez, M. A. M. Iniguez, and F. R. Luis: Nuevas fuentes de cumarinas naturales XVI. Productos de los tallos de la Ruta pinnata L. fil. estructura de la benahorina. Anales de Quím. 67, 441 (1971).

    Google Scholar 

  235. González, A. G., J. M. Trujillo, R. Estevez, and J. P. Perez: Componentes de umbelíferas IV. Lignanos del Bupleurum fruticescens L. Anales de Quím. 71, 109 (1975).

    Google Scholar 

  236. Gottlieb, O. R., M. Leao da Silva, and J. G. Soares Maia: Distribution of Coumarins in Amazonian Brosimum Species. Phytochemistry 11, 3479 (1972).

    CAS  Google Scholar 

  237. Govindachari, T. R., B. R. Pai, P. S. Subramaniam, and N. Muthukumaraswamy: Coumarins of Clausena dentata (Willd.) R. and S. Tetrahedron 24, 753 (1968).

    Google Scholar 

  238. Govindachari, T. R., B. R. Pai, P. S. Subramaniam, U. R. Rao, and N. Muthuku­maraswamy: Constituents of Mesua ferrea L. — II. Ferruol A, a New 4-Alkyl- coumarin. Tetrahedron 23, 4161 (1967).

    CAS  Google Scholar 

  239. Gray, A. I., R. D. Waigh, and P. G. Waterman: Determination of Substitution Pattern in Coumarins Using a Lanthanide Shift Reagent. J. C. S. Chem. Comm. 1974, 632.

    Google Scholar 

  240. Gray, A. I., R. D. Waigh, and P. G. Waterman: Avicennol: A New Pyranocoumarin from the Root Bark of Zanthoxylum avicennae, and its Conversion into Avicennin. J. C. S. Perkin I 1975, 488.

    Google Scholar 

  241. Gray, A. I., R. D. Waigh, and P. G. Waterman: cis-Avicennol, a New Pyranocoumarin from the Root Bark of Zanthoxylum elephantiasis. Phytochemistry 16, 1017 (1977).

    CAS  Google Scholar 

  242. Grigg, R., J. A. Knight, and P. Roffey: NMR Solvent Shifts and Structure Elucidation in Coumarins. Tetrahedron 22, 3301 (1966).

    CAS  Google Scholar 

  243. Grisebach, H., and W. D. Ollis: Biogenetic Relationship between Coumarins, Flavonoids, Isoflavonoids and Rotenoids. Experientia 17, 4 (1961).

    CAS  Google Scholar 

  244. Guiotto, A., P. Rodighiero, and U. Quintily: Poncimarin, a New Coumarin from Poncirus trifoliata L. Z. Naturforsch. 30c, 420 (1975).

    CAS  Google Scholar 

  245. Guiotto, A., P. Rodighiero, U. Quintily, and G. Pastorini: Isoponcimarin: New Coumarin from Poncirus trifoliata. Phytochemistry 15, 348 (1976).

    CAS  Google Scholar 

  246. Guise, G. B., E. Ritchie, R. G. Senior, and W. C. Taylor: The Chemical Consti­tuents of Australian Zanthoxylum Species IV. Two New Coumarins from Z. subero- sum C. T. White (syn. Z. dominianum Merr. and Perry; Z. ovalifolium Wight). Austral. J. Chem. 20, 2429 (1967).

    CAS  Google Scholar 

  247. Gupta, B. D., S. K. Banerjee, K. L. Handa, and C. K. Atal: Heratomin and Heratomol, New Coumarins from Heracleum thomsoni. Phytochemistry 15, 1319 (1976).

    CAS  Google Scholar 

  248. Gupta, B. D., B. K. Wali, Vishwapaul, and K. L. Handa: Coumarins from Prangos pabularia Lindl. Indian J. Chem. 2, 464 (1964).

    CAS  Google Scholar 

  249. Hahn, D. R.: Biochemical Studies on the Constituents of Artemisia messerschmidiana and their Derivatives. I. Identification of Esculetin Methyl Ethers and their cholagogic Action. Yakhak Hoeji 10, 20 (1966); Chem. Abs. 68, 112202 (1968).

    Google Scholar 

  250. Halpern, O., P. Waser, and H. Schmid: Die Konstitution des Athamantins und des Oroselols. Helv. Chim. Acta 40, 758 (1957).

    CAS  Google Scholar 

  251. Harada, I., Y. Hirose, and M. Nakazaki: The Absolute Configurations of (+)- Marmesin and (—)-Hydroxytremetone. Tetrahedron Letters 1968, 5463.

    Google Scholar 

  252. Hasegawa, M.: Flavonoids of Various Prunus Species X. Wood Constituents of Prunus tomentosa. Bot. Mag. Tokyo 82, 458 (1969); Chem. Abs. 73, 956 (1970).

    Google Scholar 

  253. Hata, K.: Studies on the Chemical Components of Umbelliferous Plants II. Com­ponents of Angelica glabra Makino (2). Yakugaku Zasshi 76, 666 (1956); Chem. Abs. 51, 1152 (1957).

    Google Scholar 

  254. Hata, K., and M. Kozawa: The Constitution of Angelol, a New Coumarin Isolated from the Root of Angelica pubescens Maxim. ( Umbelliferae ). Tetrahedron Letters 1965, 4557.

    Google Scholar 

  255. Hata, K., and M. Kozawa: The Formation of Angelical from Angelol, a New Coumarin Isolated from the Root of Angelica pubescens Maxim. (Umbelliferae). Yakugaku Zasshi 87, 210 (1967); Chem. Abs. 67, 43633 (1967).

    Google Scholar 

  256. Hata, K., and M. Kozawa: Studies on Coumarins from the Root of Angelica pubescens Maxim I. The Structure of Angelol. Yakugaku Zasshi 88, 283 (1968); Chem. Abs. 69, 59041 (1968).

    Google Scholar 

  257. Hata, K., and M. Kozawa: Studies on Coumarins from the Root of Angelica pubescens Maxim II. Absolute Configuration of Angelol. Yakugaku Zasshi 88, 293 (1968); Chem. Abs. 69, 59039 (1968).

    Google Scholar 

  258. Hata, K., M. Kozawa, and K. Baba: Coumarins from Chinese Crude Drug “She Huangzi”, the Fruits of Cnidium sp. and from Cnidium japonicum Miq. Yakugaku Zasshi 92, 1289 (1972); Chem. Abs. 78, 33845 (1973).

    Google Scholar 

  259. Hata, K., M. Kozawa, K. Baba, and M. Mitsui: Chemical Components of the Roots of Ligusticum hultenii Fernald and Angelica shikokiana Makino. Yakugaku Zasshi 93, 248 (1973); Chem. Abs. 78, 133334 (1973).

    Google Scholar 

  260. Hata, K., M. Kozawa, K. Baba, and M. Mitsui: New Ester Coumarins, Angeladin and Isoedultin from Angelica longera- diata (Maxim.) Kitagawa. Chem. and Pharm. Bull. (Japan) 21, 518 (1973).

    CAS  Google Scholar 

  261. Hata, K., M. Kozawa, K. Baba, and K.-Y. Yen: Coumarins from the Roots of Angelica laxiflora Diels. Chem. and Pharm. Bull. (Japan) 19, 640 (1971).

    CAS  Google Scholar 

  262. Hata, K., M. Kozawa, and Y. Ikeshiro: The Constitution of Anomalin, a New Coumarin Isolated from the Root of Angelica anomala Lall (Umbelliferae). Chem. and Pharm. Bull. (Japan) 14, 94 (1966).

    CAS  Google Scholar 

  263. Hata, K., M. Kozawa, and Y. Ikeshiro: New Coumarins Isolated from the Roots of Angelica anomala and A. cartilaginomarginata. Yakugaku Zasshi 87, 1118 (1967); Chem. Abs. 68, 10231 (1968).

    Google Scholar 

  264. Hata, K., M. Kozawa, Y. Ikeshiro, and K.-Y. Yen: New Coumarins Isolated from the Root of Peucedanum formosanum Hayata and Peucedanum japonicum Thunb. Yakugaku Zasshi 88, 513 (1968); Chem. Abs. 69, 96521 (1968).

    Google Scholar 

  265. Hata, K., M. Kozawa, and K.-Y. Yen: The Constitution of Peuformosin, a New Coumarin Isolated from the Root of Peucedanum formosanum Hayata (Umbelliferae). Chem. and Pharm. Bull. (Japan) 14, 442 (1966).

    CAS  Google Scholar 

  266. Hata, K., and K. Sano: The Constitution of Decursin, a New Coumarin Isolated from the Root of Angelica decursiva Fr. et Sav. ( Umbelliferae ). Tetrahedron Letters 1966, 1461.

    Google Scholar 

  267. Hata, K., and K. Sano: Studies on Coumarins from the Root of Angelica decursiva Fr. et Sav. I. The Structure of Decursin and Decursidin.Yakugaku Zasshi 89, 549 (1969); Chem. Abs. 71, 38832 (1969).

    Google Scholar 

  268. Hata, K., and Y. Tanaka: Chemical Components of Umbelliferous Plants III. Components of the Root of Angelica pubescens. I. Yakugaku Zasshi 77, 937 (1958); Chem. Abs. 52, 3799 (1960).

    Google Scholar 

  269. Head, F. S. H., and A. Robertson: Natural Glucosides. Part II. The Constitution of Aesculin. J. Chem. Soc. 1930, 2434.

    Google Scholar 

  270. Hegarty, M. P., and F. N. Lahey: The Coumarins of Halfordia scleroxyla F. Muell. Austral. J. Chem. 9, 120 (1956).

    CAS  Google Scholar 

  271. Herz, W., S. V. Bhat, and P. S. Santhanam: Coumarins of Artemisia dracunculoides and 3’,6-Dimethoxy-4’,5,7-trihydroxyflavone in A. arctica. Phytochemistry 9, 891 (1970).

    CAS  Google Scholar 

  272. Hlubucek, J., E. Ritchie, and W. C. Taylor: Synthesis of 2,2-Dimethylchromenes. Tetrahedron Letters 1969, 1369.

    Google Scholar 

  273. Hlubucek, J., E. Ritchie, and W. C. Taylor: Synthesis of 2,2-Dimqthylchromenes. Austral. J. Chem. 24, 2347 (1971).

    CAS  Google Scholar 

  274. Hlubucek, J., E. Ritchie, and W. C. Taylor: Synthesis of o-Isopentenylphenols. Austral. J. Chem. 24, 2355 (1971).

    CAS  Google Scholar 

  275. Hörhammer, L., H. Wagner, and W. Eyrich: Über die Inhaltsstoffe der Früchte von Angelica silvestris L. Z. Naturforsch. 18b, 639 (1963).

    Google Scholar 

  276. Hörhammer, L., H. Wagner, and D. Kraemer-He yd weiler: Neue Methoden im Pharmakognostischen Unterricht (12. Mitteilung): Identifizierung von Umbelliferen- wurzeln und Nachweis der wichtigsten Verfälschungen mit Hilfe der Dünnschicht­chromatographie. Deut. Apotheker-Ztg. 106, 267 (1966); Chem. Abs. 65, 2065 (1966).

    Google Scholar 

  277. Ignat’eva, N. S., V. V. Vandyshev, and M. G. Pimenov: Coumarins from the Roots of Cachrys pubescens. Khim. prirod. Soedinenii 8, 388 (1972); Chem. Abs. 77, 149704 (1972).

    Google Scholar 

  278. Irie, H., S. Uyeo, K. Yamomoto, and K. Kinoshita: The Structure of Glaupalol, a Novel Furocoumarin from Glaucidium palmatum Sieb, et Zucc. Chem. Comm. 1967, 547.

    Google Scholar 

  279. Ishii, H., and K. Hosoya: Arnottianin, a New Dihydropyranocoumarin. Chem. and Pharm. Bull. (Japan) 20, 860 (1972).

    CAS  Google Scholar 

  280. Ishii, H., K. Hosoya, T. Ishikawa, and J. Haginiwa: Studies on the Chemical Constituents of Rutaceous Plants. XX. The Chemical Constituents of Xanthoxylum arnottianum Maxim. (1). Isolation of the Chemical Constituents of the Xylem of Roots. Yakugaku Zasshi 94, 309 (1974); Chem. Abs. 81, 132752 (1974).

    Google Scholar 

  281. Ishii, H., K. Hosoya, T. Ishikawa, E. Ueda, and J. Haginiwa: Studies on the Chemical Constituents of Rutaceous Plants. XXI. The Chemical Constituents of Xanthoxylum arnottianum Maxim. (2). Isolation of the Chemical Constituents of the Xylem of Stems. Yakugaku Zasshi 94, 322 (1974); Chem. Abs. 81, 132753 (1974).

    Google Scholar 

  282. Ishii, H., and T. Ishikawa: Arnottinin: Structure Establishment by Chemical Correlation with Osthenol. Chem. and Pharm. Bull. (Japan) 23, 934 (1975).

    CAS  Google Scholar 

  283. Ishii, H., T. Ishikawa, H. Sekiguchi, and K. Hosoya: Xanthoarnol: A New Dihydrofuranocoumarin. Chem. and Pharm. Bull. (Japan) 21, 2346 (1973).

    CAS  Google Scholar 

  284. Janot, M. M., J. Le Men, H. Pourrat, and V. Plouvier: Constitution du calycanthoside. Bull. Soc. chim. Biol. 37, 365 (1955).

    CAS  Google Scholar 

  285. Jarvis, M. W., and A. G. Moritz: Long-Range Coupling in Substituted Coumarins. Austral. J. Chem. 21, 2445 (1968).

    CAS  Google Scholar 

  286. Jefferies, P. R., and G. K. Worth: The Chemistry of the Western Australian Rutaceae — VI. Two Novel Coumarins from Eriostemon brucei. Tetrahedron 29, 903 (1973).

    CAS  Google Scholar 

  287. Jensen, S. R., and B. J. Nielsen: A New Coumarin, Fraxidin 8-O-β-D-glucoside and 10-Hydroxyligstroside from Bark of Fraxinus exelsior. Phytochemistry 15, 221 (1976).

    CAS  Google Scholar 

  288. Joshi, B. S., and D. H. Gawad: Isolation of Some Furanocoumarins from Clausena indica and Identity of Chalepensin with Xylotenin. Phytochemistry 10, 480 (1971).

    CAS  Google Scholar 

  289. Joshi, B. S., and V. N. Kamat: Structures of Clausenin, Clausenidin and a Synthesis of Clausenin and Xanthoxyletin. Tetrahedron Letters 1966, 5767.

    Google Scholar 

  290. Joshi, B. S., V. N. Kamat, and D. H. Gawad: Structure of Clausindine, a New Coumarin from Clausenia indica Oliv. Experientia 30, 223 (1974).

    CAS  Google Scholar 

  291. Joshi, B. S., V. N. Kamat, and D. H. Gawad: Clausidine, a Novel Cyclopropylcoumarin. J. C. S. Perkin I 1974, 1561.

    Google Scholar 

  292. Joshi, B. S., V. N. Kamat, T. R. Govindachari, and A. K. Ganguly: Isolation and Structure of Surangin A and Surangin B, Two New Coumarins from Mammea longifolia (Wight) Planch and Triana. Tetrahedron 25, 1453 (1969).

    CAS  Google Scholar 

  293. Joshi, B. S., V. N. Kamat, and A. K. Saksena: Structures of Clausenin and Clausenidin, Two New Pyranocoumarins from the Roots of Clausena heptaphylla Wt. and Arn. Tetrahedron 23, 4785 (1967).

    CAS  Google Scholar 

  294. Joshi, B. S., Y. N. Shukla, D. S. Bhakuni, and M. M. Dhar: 6-(2,3-Dihydroxy- 3-methylbutyl)-7-methoxycoumarin, a New Coumarin from Micromelum pubescens Blume. Indian J. Chem. 13, 772 (1975).

    CAS  Google Scholar 

  295. Kadyrov, A. S., A. I. Saidkhodzhaev, and G. K. Nikonov: The Structures of Feroside and of Reoselin A, New Glycosides from the Roots of Ferula korshinskyi. Khim. prirod. Soedinenii 11, 574 (1975); Chem. Abs. 84, 74568 (1976).

    Google Scholar 

  296. Kamilov, K. M, V. V. Kiseleva, and G. K. Nikonov: Diversoside, a New Coumarin from the Roots of Ferula diversivitatta. Khim. prirod. Soedinenii 10, 781 (1974); Chem. Abs. 82, 135684 (1975).

    Google Scholar 

  297. Kamilov, K. M., and G. K. Nikonov: Coumarins of Ferula kopetdaghensis and the Structure of Kopeolin and Kopeoside. Khim. prirod. Soedinenii 9, 308 (1973); Chem. Abs. 79, 134321 (1973).

    Google Scholar 

  298. Kamilov, K. M., and G. K. Nikonov: Structure of the Coumarin Reoselin. Khim. prirod. Soedinenii 10, 84 (1974); Chem. Abs. 80, 121275 (1974).

    Google Scholar 

  299. Kamilov, K. M., and G. K. Nikonov: Kamolone from the Roots of Ferula kopetdaghensis. Khim. prirod. Soedinenii 10, 85 (1974); Chem. Abs. 81, 60806 (1974).

    Google Scholar 

  300. Kamilov, K. M., and G. K. Nikonov: Coumarins of Ferula kopetdaghensis — Kopetdaghin and Kopeodin (Farnesiferol B). Khim. prirod. Soedinenii 10, 442 (1974); Chem. Abs. 82, 70266 (1975).

    Google Scholar 

  301. Kapoor, S. L., Y. N. Sharma, and A. Zaman: Extractives of Angelica glauca. Phytochemistry 11, 475 (1972).

    CAS  Google Scholar 

  302. Kariyone, T., and K. Hata: Studies on the Chemical Components of Umbelliferous Plants I. Components of the Roots of Angelica glabra Makino. Yakugaku Zasshi 76, 649 (1956); Chem. Abs. 51, 1152 (1957).

    Google Scholar 

  303. Kariyone, T., and T. Matsuno: Studies on the Constituents of Orange Oil. I. On the Structure of Auraptene. Pharm. Bull. (Japan) 1, 119 (1953).

    CAS  Google Scholar 

  304. Karrer, W.: In: Konstitution und Vorkommen der organischen Pflanzenstoffe. 531. Basel: Birkhäuser. 1958.

    Google Scholar 

  305. Khaled, S. A., K. Szendrei, I. Noväk, and J. Reisch: Coumarin Glycosides from Peucedanum ostruthium. Phytochemistry 14, 1461 (1975).

    CAS  Google Scholar 

  306. Khanna, P. L., and T. R. Seshadri: Synthesis of Isoprenoid Polyphenols. J. Sci. Ind. Res., India 33, 295 (1974).

    CAS  Google Scholar 

  307. Khasanov, T. K., A. I. Saidkhodzhaev, and G. K. Nikonov: Structure and Configuration of New Coumarins of the Roots of Ferula mogoltavica Khim. prirod. Soedinenii 10, 10 (1974); Chem. Abs. 80, 121131 (1974).

    Google Scholar 

  308. Structure and Configuration of the Coumarins Mogoltadone and Mogoltadin. Khim. prirod. Soedinenii 10, 25 (1974); Chem. Abs. 80, 121138 (1974).

    Google Scholar 

  309. Khasanov, T. K., A. I. Saidkhodzhaev, and G. K. Nikonov: Structure and Configuration of Polyanthin and Polyanthinin — New Coumarins from the Roots of Ferula polyantha. Khim. prirod. Soedinenii 10, 517 (1974); Chem. Abs. 82, 95266 (1975).

    Google Scholar 

  310. Structure of Feropolin, Feropolol, Feropolone, and Feropolidin. Khim. prirod. Soedinenii 12, 91 (1976); Chem. Abs. 85, 59558 (1976).

    Google Scholar 

  311. Structure of Mogoltacin. Khim. prirod. Soedinenii 12, 95 (1976); Chem. Abs. 85, 59561 (1976).

    Google Scholar 

  312. Khosa, R. L.: Coumarins from the Leaves of Murraya paniculata. Indian J. Pharm. 34, 47 (1972).

    CAS  Google Scholar 

  313. Khosa, R. L.: Structure of a New Coumarin from Murraya paniculata. Indian J. Pharm. 37, 43 (1975).

    CAS  Google Scholar 

  314. Khosa, R. L.: Kiangsu Luminescent Bacteria Research Unit: Armillariella tabescens. II. Isolation and the Structure of the Armillarisins. Sci. Sinica 17, 377 (1974); Chem. Abs. 82, 1919 (1975).

    Google Scholar 

  315. Kikuchi, T., T. Yokoi, K. Umemoto, and T. Shingu: Constituents of Scaevola frutescens (Miller) Krause. Yakugaku Zasshi 94, 1616 (1974); Chem. Abs. 82, 135677 (1975).

    Google Scholar 

  316. Kincl, F. A., J. Romo, G. Rosenkranz, and F. Sondheimer: The Constituents of Casimiroa edulis Llave et Lex. Part 1. The Seed. J. Chem. Soc. 1956, 4163.

    Google Scholar 

  317. King, F. E., J. R. Housley, and T. J. King: The Chemistry of Extractives from Hardwoods. Part XVI. Coumarin Constituents of Fagara macrophylla, Zanthoxylum flavum, and Chloroxylon swietenia. J. Chem. Soc. 1954, 1392.

    Google Scholar 

  318. Kinoshita, K., and S. Murase: The Structure of eis- and /rafw-Glaupadiol. (Studies on the Constituents of the Rhizomes of Glaucidium palmatum Sieb, and Zucc.) Yakugaku Zasshi 93, 202 (1973); Chem. Abs. 78, 136129 (1973).

    Google Scholar 

  319. Kir’yalov, N. P.: The Structure of Cocanicine and Umbelliprenin, Components of the Neutral Part of Oil from Ferula cocanica. Trudy bot. Inst. Akad. Nauk S.S.S.R. 8, 7 (1961); Chem. Abs. 58, 498 (1963).

    Google Scholar 

  320. Kir’yalov, N. P.: Coumarins from Plants of the Genus Ferula. Trudy bot. Inst. Akad. Nauk S.S.S.R. 12, 82 (1965); Chem. Abs. 64, 3461 (1966).

    Google Scholar 

  321. Kir’yalov, N. P.: Isolation of the Coumarin Badrakemin from the Roots of Ferula badrakema. Khim. prirod. Soedinenii 3, 363 (1967); Chem. Abs. 69, 35865 (1968).

    Google Scholar 

  322. Kir’yalov, N. P.: The Coumarin Diversine from the Roots of Ferula diversivittata. Khim. prirod. Soedinenii 5, 51 (1969); Chem. Abs. 70, 118026 (1969).

    Google Scholar 

  323. Kir’yalov, N. P., and V. Y. Bagirov: Structure of Karatavicin. Khim. prirod. Soedinenii 3, 223 (1967); Chem. Abs. 68, 68829 (1968).

    Google Scholar 

  324. Kir’yalov, N. P., and V. Y. Bagirov: The Structure of Karatavic Acid. Khim. prirod. Soedinenii 4, 283 (1968); Chem. Abs. 70, 77715 (1969).

    Google Scholar 

  325. Kir’yalov, N. P., and V. Y. Bagirov: The Structure of Karatavicinol. Khim. prirod. Soedinenii 5, 225 (1969); Chem. Abs. 72, 55164 (1970).

    Google Scholar 

  326. Kir’yalov, N. P., and T. V. Bukreeva: A New Coumarin from the Roots of Ferula pseudooreoselinum. Khim. prirod. Soedinenii 8, 643 (1972); Chem. Abs. 78,108210 (1973).

    Google Scholar 

  327. Samarcandin Acetate from the Roots of Ferula pseudooreoselinum. Khim. prirod. Soedinenii 8, 798 (1972); Chem. Abs. 78, 108250 (1973).

    Google Scholar 

  328. Coumarins from the Roots of Ferula pseudooreoselinum. Khim. prirod. Soedinenii 9, 425 (1973); Chem. Abs. 79, 134324 (1973).

    Google Scholar 

  329. Kir’yalov, N. P., T. V. Bukreeva, V. A. Gindin, G. Mamatov, and I. S. Kozhina: The Structure of the Coumarin Glucoside Reoselin from the Roots of Ferula pseudooreoselinum. Khim. prirod. Soedinenii 11, 87 (1975); Chem. Abs. 83, 97826 (1975).

    Google Scholar 

  330. Kir’yalov, N. P., and S. D. Movchan: A New Glycoside, Reoseline from the Rosin of the Roots of Ferula pseudooreoselinum. Doklady Akad. Nauk. S.S.S.R. 148, 1081 (1963); Chem. Abs. 59, 5255 (1963).

    Google Scholar 

  331. Kir’yalov, N. P., and V. Y. Bagirov: The Structure of Gummosin. Khim. prirod. Soedinenii 2, 383 (1966); Chem. Abs. 67, 11394 (1967).

    Google Scholar 

  332. The Structure of Samarcandin and Samarcandone, Coumarin Compounds from Ferula samarcandica. Khim. prirod. Soedinenii 4, 73 (1968); Chem. Abs. 69, 59040 (1968).

    Google Scholar 

  333. Kiseleva, V. V., G. K. Nikonov, and M. O. Karryev: Structure of Diversin and Diversinin, Coumarins of Ferula diversivittata. Khim. prirod. Soedinenii 11, 344 (1975); Chem. Abs. 84, 28001 (1976).

    Google Scholar 

  334. Komatsu, S., S. Tanaka, S. Ozawa, R. Kubo, Y. Ono, and Z. Matsuda: Biochemical Studies on Grape Fruits, Citrus aurantium L. J. Chem. Soc. Japan 51, 478 (1930).

    CAS  Google Scholar 

  335. Komissarenko, N. F., and V. T. Chernobai: Furocoumarins of Cnidium dubium. Khim. prirod. Soedinenii 2, 375 (1966); Chem. Abs. 67, 11395 (1967).

    Google Scholar 

  336. Konoshima, M., H.-J. Chi, and K. Hata: Coumarins from the Root of Angelica gigas Nakai. Chem. Pharm. Bull. (Japan) 16, 1139 (1968).

    CAS  Google Scholar 

  337. Krivut, B. A., L. G. Avramenko, M. E. Perel’son, and G. K. Nikonov: Preparation and Quantitative Determination of Benzoylmarmesin. Khim. prirod. Soedinenii 6, 526 (1970); Chem. Abs. 74, 53420 (1971).

    Google Scholar 

  338. Kuffner, F., A. Nikiforov, and G. Schulz: Über das Rutolid. Monatsh. 104, 911 (1973).

    CAS  Google Scholar 

  339. Kutney, J. P., G. Eigendorf, T. Inaba, and D. L. Dreyer: Mass Spectral Frag­mentation Studies in Monomeric and Dimeric Coumarins. Org. Mass Spectrom. 5, 249 ( 1970.

    Google Scholar 

  340. Kutney, J. P., P. J. Salisbury, and A. K. Verma: Biosynthetic Studies in the Coumarin Series — III. Studies in Tissue Cultures of Thamnosma montana Torr, and Frem. The Role of Mevalonate. Tetrahedron 29, 2673 (1973).

    CAS  Google Scholar 

  341. Kutney, J. P., A. K. Verma, and R. N. Young: Studies on Constituents of Thamnosma montana Torr, and Frem. The Structure of Thamnosmin, a Novel Coumarin Epoxide. Tetrahedron 28, 5091 (1972).

    CAS  Google Scholar 

  342. Biosynthetic Studies in the Coumarin Series — I. Studies in Plants of Thamnosma montana Torr, and Frem. The Role of Mevalonate. Tetrahedron 29, 2645 (1973).

    Google Scholar 

  343. Biosynthetic Studies in the Coumarin Series — II. Studies in Plants of Thamnosma montana Torr, and Frem. The Role of Acetate and Glycine. Tetrahedron 29, 2661 (1973).

    Google Scholar 

  344. Kutney, J. P., R. N. Young, and A. K. Verma: Novel Epoxides from Thamnosma montana Torr, and Frem. Tetrahedron Letters 1969, 1845.

    Google Scholar 

  345. Kuznetsova, G. A.: Discovery of Imperatorin Oxide in Plants. Zhur. obshchei Khim. 35, 403 (1965); Chem. Abs. 62, 15071 (1965).

    Google Scholar 

  346. Kuznetsova, G. A.: Natural Coumarins and Furocoumarins: Leningrad: Nauka. 1967; Chem. Abs. 67, 108551 (1967).

    Google Scholar 

  347. Kuznetsova, G. A., and A. Z. Abyshev: Natural (-)-7-Methoxy-8-(β,γ-dihydro- xyisopentyl)-coumarin. Khim. prirod. Soedinenii 1, 283 (1965); Chem. Abs. 64, 683 (1966).

    Google Scholar 

  348. Kuznetsova, G. A., and A. Z. Abyshev: Merancin Hydrate — A Component of the Roots of Prangos ferulacea (L.) Lindl. Zhur. priklad. Khim. 38, 2370 (1965); Chem. Abs. 64, 2326 (1966).

    Google Scholar 

  349. Kuznetsova, G. A., A. Z. Abyshev, M. E. Perel’son, Y. N. Sheinker, and G. Y. Pek: A New Coumarin, Pranferol, from the Roots of Prangos ferulacea. Khim. prirod. Soedinenii 2, 310 (1966); Chem. Abs. 66, 94923 (1967).

    Google Scholar 

  350. Kuznetsova, G. A., and L. M. Belenovskaya: A Chemical Study of the Roots of Prangos ornata Kuzm. Khim. prirod. Soedinenii 1, 430 (1965); Chem. Abs. 64, 13088 (1965).

    Google Scholar 

  351. Kuznetsova, G. A., and L. M. Belenovskaya: Isolation of Oxypeucedanin Hydrate (Prangol) from the Roots of Prangos fedtschenkoi (Rgl. et Schmal.) Eug. Kor. Zhur. priklad. Khim. 38, 1146 (1965); Chem. Abs. 63, 6021 (1965).

    Google Scholar 

  352. Kuznetsova, G. A., and L. M. Belenovskaya: Prantschimgin, a New Coumarin from the Roots of Prangos tschimganica. Khim. prirod. Soedinenii 2, 235 (1966); Chem. Abs. 66, 2438 (1967).

    Google Scholar 

  353. Kuznetsova, G. A., and L. M. Belenovskaya: Additional Information on the Coumarin Composition of Prangos fedtschenkoi (Regel et Schmalh). Korob., P. tschimganica B. Fedtsch and P. isphairamica B. Fedtsch. (Umbelliferae). Zhur. priklad. Khim. 42, 471 (1969); Chem. Abs. 71, 811 (1969).

    Google Scholar 

  354. Kuznetsova, G. A., and V. N. Florya: Coumarins from the Roots, Aboveground Parts, and Fruits of Seseli campestre Growing in Moldavia. Zhur. priklad. Khim. 43, 1412 (1970); Chem. Abs. 73, 117214 (1970).

    Google Scholar 

  355. Kuznetsova, G. A., and N. F. Gashimov: The Structure of a New Coumarin from Haplophyllum pedicellatum. Khim. prirod. Soedinenii 8, 666 (1972); Chem. Abs. 78, 108171 (1973).

    Google Scholar 

  356. Kuznetsova, G. A., and N. F. Gashimov: A New Coumarin, Pedicellone from Haplophyllum pedicellatum. Khim. prirod. Soedinenii 9, 113 (1973); Chem. Abs. 79, 5223 (1973).

    Google Scholar 

  357. Kuznetsova, G. A., and G. V. Pigulevskii: The Structure of Prangenine. Zhur. obshchei Khim. 31, 323 (1961); Chem. Abs. 55, 22282 (1961).

    Google Scholar 

  358. Kuznetsova, G. A., and L. M. Sokolova: Coumarins from the Roots of PrangosNaturally Occurring Plant Coumarins fedtschenkoi (Rgl. et Schmalh.) Eug. Kor. Zhur. priklad. Khim. 37, 1105 (1964); Chem. Abs. 61, 4630 (1964).

    Google Scholar 

  359. Kuznetsova, G. A., and A. D. Zorina: Coumarins from the Roots of Prangos serawschanica (Rgl. et Schmalh.) Korov. Zhur. priklad. Khim. 39, 482 (1966); Chem. Abs. 65, 1043 (1966).

    Google Scholar 

  360. Lahey, F. N., and J. K. MacLeod: The Coumarins of Geijera parviflora Lindi. Austral. J. Chem. 20, 1943 (1967).

    CAS  Google Scholar 

  361. Halfordin and Isohalfordin — Revised Structures. Tetrahedron Letters 1968, 447.

    Google Scholar 

  362. Lahey, F. N., and D. J. Wluka: Geijerin, a New Coumarin from the Bark of Geijera salicifolia Schott. Austral. J. Chem. 8, 125 (1955).

    CAS  Google Scholar 

  363. Lamberton, J. A., J. R. Price, and A. H. Redcliffe: Micromelin, a New Coumarin from Micromelum minutum (Forst. f.) Seem (Family Rutaceae). Austral. J. Chem. 20, 973 (1967).

    CAS  Google Scholar 

  364. Lapper, R. D.: The Carbon-13 Nuclear Magnetic Resonance Spectrum of Siderin. Tetrahedron Letters 1974, 4293.

    Google Scholar 

  365. Larsen, P. K., and F. Sandberg: Constituents of Umbelliferous Plants. XV. Cou­marins from Thapsia garganica L. The Structure of a New Coumarin. Acta Chem. Scand. 24, 1113 (1970).

    CAS  Google Scholar 

  366. Lassak, E. V., and J. T. Pinhey: The Constituents of Eriostemon trachyphyllus. The Structure of Trachyphyllin, a New Coumarin. Austral. J. Chem. 22, 2175 (1969).

    CAS  Google Scholar 

  367. Lassak, E. V., and I. A. Southwell: The Coumarins from the Resin of Evodia vitiflora. Austral. J. Chem. 25, 2491 (1972).

    CAS  Google Scholar 

  368. Laxmi, M. V., C. V. Ratnam, and N. V. Subba Rao: 7-Methoxy-8-(3-butenyl-3- methyl-2-oxo)-coumarin, a New Coumarin from Murraya exotica Linn. Indian J. Chem. 10, 564 (1972).

    Google Scholar 

  369. Lee, K.-H., and T. O. Soine: Coumarins VII: The Coumarins of Lomatium nuttalli. J. Pharm. Sci. 57, 865 (1968).

    CAS  Google Scholar 

  370. Lee, K.-H., and T. O. Soine: Coumarins IX: Coumarins of Spheriosciadium capitellatum (A. Gray). J. Pharm. Sci. 58, 675 (1969).

    CAS  Google Scholar 

  371. Lee, K.-H., and T. O. Soine: Coumarins X: Spectral Studies on Some Linear Furocoumarins. J. Pharm. Sci. 58, 681 (1969).

    CAS  Google Scholar 

  372. Lemmich, E., J. Lemmich, and B. E. Nielsen: Constituents of Umbelliferous Plants XIV. Coumarins of Peucedanum oreoselinum (L.) Moench. Acta Chem. Scand. 24, 2893 (1970).

    CAS  Google Scholar 

  373. Lemmich, J., E. Lemmich, and B. E. Nielsen: Constituents of Umbelliferous Plants VIII. Coumarins from the Root of Seseli libanotis (L.) Koch. The Structure of Three New Coumarins. Acta Chem. Scand. 20, 2497 (1966).

    CAS  Google Scholar 

  374. Lemmich, J., and B. E. Nielsen: Constituents of Umbelliferous Plants (X). Stereo­chemistry of Natural Coumarins Containing the 3-Hydroxy-2,2-dimethylchroman System. Tetrahedron Letters 1969, 3.

    Google Scholar 

  375. Lemmich, J., P. A. Pedersen, and B. E. Nielsen: Revised Absolute Configurations of Natural Khellactone Esters (1). Tetrahedron Letters 1969, 3365.

    Google Scholar 

  376. Lemmich, J., P. A. Pedersen, and B. E. Nielsen: Constituents of Umbelliferous Plants XVIII. Terpenoids and Coumarins of the Root of Ligusticum seguieri Koch. Acta Chem. Scand. 25, 344 (1971).

    CAS  Google Scholar 

  377. Coumarins and Terpenoids of the Fruits of Ligusticum seguieri. Phytochemistry 10, 3333 (1971).

    Google Scholar 

  378. McCabe, P. H., R. McCrindle, and R. D. H. Murray: Constituents of Sneezewood, Ptaeroxylon obliquum (Thunb.) Radlk. Part I. Chromones. J. Chem. Soc. (C) 1967, 145.

    Google Scholar 

  379. McLeod, J. K.: Halfordinin, a 3,4,5-Oxygenated Furocoumarin with a Novel α, α - Dimethylallyl Ether Substituent. Tetrahedron Letters 1970, 1319.

    Google Scholar 

  380. McLeod, J. K.: Halfordinin — A Revised Structure. Tetrahedron Letters 1970, 3611. Fortschritte d. Chem. org. Naturst. 35

    Google Scholar 

  381. Mahey, S., T. R. Seshadri, and S. K. Mukerjee: Synthesis of Poncitrin. Indian J. Chem. 11, 983 (1973).

    CAS  Google Scholar 

  382. Mahey, S., T. R. Seshadri, and S. K. Mukerjee: Nuclear Prenylation of 5,7-Dihydroxycoumarin. Synthesis of Coumurrayin and Toddaculin. Indian J. Chem. 12, 29 (1974).

    CAS  Google Scholar 

  383. Martinez, E. A., R. E. Reyes, A. G. González, and F. R. Luis: Nuevas fuentes de cumarinas naturales VIII. Cumarinas de las raíces de la Pimpinella rupicola Svent. (Umbelliferae); estructura de una nueva cumarina. Anales de Quím. 63, 205 (1967).

    Google Scholar 

  384. Matsumoto, T., K. Fukui, and M. Nanbu: Synthesis and Absolute Configuration of trans-Meranzinic Acid. Chem. Letters 1974, 603.

    Google Scholar 

  385. Mendez, J., and M. I. Lojo: Spectral Characterization of Coumarins and Cinnamic Acids. Microchem. J. 14, 567 (1969).

    CAS  Google Scholar 

  386. Mitsuhashi, H., and T. Itoh: Studies on the Constituents of Umbelliferous Plants. V. Studies on the Constituents of Angelica edulis Mayabe (1). Isolation of Edultin. Chem. and Pharm. Bull. (Japan) 10, 511 (1962).

    CAS  Google Scholar 

  387. Mitsuhashi, H., and T. Itoh: Studies on the Constituents of Umbelliferous Plants. VI. Studies on the Constituents of Angelica edulis Muyabe. (2). Chem. and Pharm. Bull. (Japan) 10, 514 (1962).

    Google Scholar 

  388. Molho, D. P., P. Jôssang, and J. Carbonnier: Structure de la sprengelianine, dihydro- furannocoumarine extraite de deux Heracleum indiens: H. ceylanicum Gardn. et H. sprengelianum W. et A. Bull. Soc. chim. France 1972, 208.

    Google Scholar 

  389. Molho, D., P. Jössang, M.-C. Jarreau, andJ. Carbonnier: Dérivés furannocoumari- niques du genre Heracleum et plus spécialement de Heracleum sprengelianum Wight et Arn. et Heracleum ceylanicum Gardn. ex C. B. Clarke. Etude Phylogénique. In: The Biology and Chemistry of the Umbelliferae (V. H. Heywood, Ed.) 337. London: Academic Press. 1971.

    Google Scholar 

  390. Mondon, A., and H. Callsen: Inhaltsstoffe der Cneoraceen, IV. Chromone und Cumarine aus Cneorwn pidverulentum. Chem. Ber. 108, 2005 (1975).

    Google Scholar 

  391. Mondon, A., H. Callsen, and P. Hartmann: Inhaltsstoffe der Cneoraceen, III. Treimverfahren fur Cneorwn pulverulentum und Untersuchung der Wachsfraktion und Phytosterole. Chem. Ber. 108, 1989 (1975).

    CAS  Google Scholar 

  392. Morris, M. P., and C. Pagán: The Isolation of the Toxic Principles of Mamey. J. Amer. Chem. Soc. 75, 1489 (1953).

    CAS  Google Scholar 

  393. Mow at, D., and R. D. H. Murray: Claisen Rearrangements — V. Synthesis of the Coumarins Dentatin (Ponicitrin) and Glabralactone (Angelicone). Tetrahedron 29, 2943 (1973).

    Google Scholar 

  394. Mujumdar, A. S., and R. S. Usgaonícar: Benzopyrans. Part V. Synthesis of a Linear Dihydrobenzodipyrandione Isolated from Dill and of Other Similar Benzo- dipyrandiones. J. C. S. Perkin I 1974, 2236.

    Google Scholar 

  395. Mujumdar, R. B., A. V. R. Rao, S. S. Rathi, and K. Venkataraman: Swietenone, the First Natural t-Butyl Ketone, from Chloroxylon swietenia. Tetrahedron Letters 1975, 867.

    Google Scholar 

  396. Mukhamedova, K. S., S. T. Akramov, and S. Y. Yunusov: Structure of Prangosine. Khim. prirod. Soedinenii 3, 117 (1967); Chem. Abs. 67, 54284 (1967).

    Google Scholar 

  397. Mukhamedova, K. S., S. T. Akramov, and S. Y. Yunusov: Mass-Spectrometric Study of Prangosine. Khim. prirod. Soedinenii 3, 357 (1967); Chem. Abs. 68, 105397 (1968).

    Google Scholar 

  398. Murray, R. D. H., and M. M. Ballantyne: Nieshoutol, a Sternutatory Hydroxy- coumarin from Sneezewood. Tetrahedron Letters 1969, 4031.

    Google Scholar 

  399. Murray, R. D. H., and M. M. Ballantyne: Constituents of Sneezewood, Ptaeroxylon obliquum — II. Coumarins — The Structure of Nieshoutol. Tetrahedron 26, 4473 (1970).

    CAS  Google Scholar 

  400. Murray, R. D. H., and M. M. Ballantyne: Claisen Rearrangements — I. Synthesis of the Coumarin, Pinnarin. Tetrahedron 26, 4667 (1970).

    CAS  Google Scholar 

  401. Murray, R. D. H., M. M. Ballantyne, T. C. Hogg, and P. H. McCabe: Claisen Rearrangements — VI. Synthesis of the Coumarins, Sesibiricin and Toddaculin. Tetrahedron 31, 2960 (1975).

    CAS  Google Scholar 

  402. Murray, R. D. H., M. M. Ballantyne, and K. P. Mathai: A Method to Introduce a 3,3-Dimethylallyl Unit Ortho to a Phenol. Tetrahedron Letters 1970, 243.

    Google Scholar 

  403. Murray, R. D. H., M. M. Ballantyne, and K. P. Mathai: Claisen Rearrangements — III. Convenient Syntheses of the Coumarins, Osthenol, Demethylsuberosin and Coumurrayin. Tetrahedron 27, 1247 (1971).

    CAS  Google Scholar 

  404. Murray, R. D. H., and I. T. Forbes: Syntheses of the Coumarins, Avicennol, Dipetaline and Dipetalolactone. Tetrahedron Letters 1976, 953.

    Google Scholar 

  405. Synthesis of 8-(3-Methylbut-2-enoyl)-7-methoxycoumarin, a Novel Coumarin from Ligusticum hultenii. Tetrahedron Letters 1977, 3077.

    Google Scholar 

  406. Murray, R. D. H., and T. C. Hogg: Synthesis of the Coumarin, Toddaculin. Tetrahedron Letters 1972, 185.

    Google Scholar 

  407. Murray, R. D. H., T. C. Hogg, M. M. Ballantyne, and P. H. McCabe: Synthesis of the Coumarin, Sesibiricin. Tetrahedron Letters 1971, 3317.

    Google Scholar 

  408. Murray, R. D. H., and D. Mow at: Synthesis of the Coumarin, Glabralactone. Tetrahedron Letters 1972, 2171.

    Google Scholar 

  409. Murray, R. D. H., M. Sutcliffe, and M. Hasegawa: Claisen Rearrangements — VII. Novel Reactions of the Coumarin, Tomentin. Tetrahedron 31, 2966 (1975).

    CAS  Google Scholar 

  410. Murray, R. D. H., M. Sutcliffe, and P. H. McCabe: Claisen Rearrangements — IV. Oxidative Cyclization of Two Coumarin o-Isoprenylphenols. Tetrahedron 27,2901(1971).

    Google Scholar 

  411. Musajo, L., and G. Rodighiero: Mode of Photosensitising Action of Furocoumarins. Photophysiology 7, 115 (1972).

    CAS  Google Scholar 

  412. Nakabayashi, T.: Coumarin Derivatives in Angelica saxicola — The Constitution of Calcicolin. Nippon Kagaku Zasshi 83, 182 (1962); Chem. Abs. 59, 1578 (1963).

    Google Scholar 

  413. Nakahara, H.: The Constituents of the Inner Bark of Hydrangea paniculata. I. A New Glycoside, Neohydrangin J. Fac. Sci., Niigata Univ. Ser. I 2, 63 (1955); Chem. Abs. 50, 4926 (1956).

    Google Scholar 

  414. Nakajima, M., J. Oda, and H. Fukami: Total Synthesis of Nodakenetin and Mar- mesin. Agric. and Biol. Chem. (Japan) 27, 695 (1963).

    CAS  Google Scholar 

  415. Nakayama, M.: NMR Solvent Shifts Induced by Benzene in Coumarins. I. Methoxyl Resonances. J. Sci. Hiroshima Univ. Ser. A-II 33, 205 (1969); Chem. Abs. 73, 24475 (1970).

    Google Scholar 

  416. Nakayama, M.: NMR Solvent Shifts Induced by Benzene in Coumarins. II. The Structure of Isohalfordin. J. Sci. Hiroshima Univ. Ser. A-II 33, 213 (1969); Chem. Abs. 73, 25339 (1970).

    Google Scholar 

  417. Nakayama, M., S. Fujimoto, K. Fukui, and J. K. MacLeod: The Isolation, Structure and Synthesis of Halkendin. Austral. J. Chem. 24, 209 (1971).

    CAS  Google Scholar 

  418. Nakazaki, M., Y. Hirose, and K. Ikematsu: The Absolute Configurations of Athamantin and Edultin. Tetrahedron Letters 1966, 4735.

    Google Scholar 

  419. Nayar, M. N. S., and M. K. Bhan: Coumarins and Other Constituents of Hespera- thusa crenulata. Phytochemistry 11, 3331 (1972).

    CAS  Google Scholar 

  420. Nayar, M. N. S., M. K. Bhan, and V. George: A New Coumarin in Boenning- hausenia albiflora. Phytochemistry 12, 2073 (1973).

    CAS  Google Scholar 

  421. Nielsen, B. E.: Coumarins of Umbelliferous Plants. Dan. Tidsskr. Farm. 44, 111 (1970); Chem. Abs. 74, 20314 (1971).

    Google Scholar 

  422. Nielsen, B. E.: Coumarin Patterns in the Umbelliferae. In: The Biology and Chemistry of the Umbelliferae (V. H. Heywood, Ed.), 325. London: Academic Press. 1971.

    Google Scholar 

  423. Nielsen, B. E., and E. Jensen: The Structure of Two New Coumarins from the Roots of Lomatium columbianum. Phytochemistry 15, 1049 (1976).

    CAS  Google Scholar 

  424. Nielsen, B. E., P. K. Larsen, and J. Lemmich: Constituents of Umbelliferous Plants XIII. Coumarins from Seseli gummiferum Pall. The Structure of Three New Coumarins. Acta Chem. Scand. 24, 2863 (1970).

    CAS  Google Scholar 

  425. Nielsen, B. E., P. K. Larsen, and J. Lemmich: Constituents of Umbelliferous Plants XVII. Coumarins from Seseli gummiferum Pall. The Structure of Two New Coumarins. Acta Chem. Scand. 25, 529 (1971).

    CAS  Google Scholar 

  426. Nielsen, B. E., and L. Lemmich: Constituents of Umbelliferous Plants III. The Structure of Archangelicin, a Coumarin from Angelica archangelica L. subsp. lit oralis Thell. Acta Chem. Scand. 18, 932 (1964).

    CAS  Google Scholar 

  427. Nielsen, B. E., and L. Lemmich: Constituents of Umbelliferous Plants IV. The Coumarins of Peucedanum palustre L. The Structure of a New Coumarin. Acta Chem. Scand. 18, 1379 (1964).

    CAS  Google Scholar 

  428. Nielsen, B. E., and L. Lemmich: Constituents of Umbelliferous Plants V. On the Configuration of Archangeli­cin and Related Coumarins. Acta Chem. Scand. 18, 2111 (1964).

    CAS  Google Scholar 

  429. Nielsen, B. E., and L. Lemmich: Constituents of Umbelliferous Plants VI. The Structure of Peulustrin, a New Coumarin from Peucedanum palustre L. Acta Chem. Scand. 19 601 (1965).

    CAS  Google Scholar 

  430. Nielsen, B. E., and L. Lemmich: Constituents of Umbelliferous Plants VII. Coumarins from the Fruits of Peucedanum palustre L. The Structure of Two New Coumarins. Acta Chem. Scand. 19, 1810 (1965).

    CAS  Google Scholar 

  431. Nielsen, B. E., and L. Lemmich: Constituents of Umbelliferous Plants IX. The Configuration of (+)-Oxy- peucedanin Hydrate and Related Coumarins. Acta Chem. Scand. 23, 962 (1969).

    CAS  Google Scholar 

  432. Nielsen, B. E., and T. O. Soine: Coumarins IV. Coumarins of Pteryxia terebin- thina. Structures of Two New Coumarins, Isopteryxin and Calipteryxin. J. Pharm. Sci. 56, 184 (1967).

    CAS  Google Scholar 

  433. Nigam, S. K., C. R. Mitra, G. Kunesch, B. C. Das, and J. Polonsky: Constituents of Calophyllum tomentosum and Calophyllum apetalum Nuts: Structure of a New 4-Alkyl- and of Two 4-Phenyl-Coumarins. Tetrahedron Letters 1967, 2633.

    Google Scholar 

  434. Nikonov, G. K.: Deltoin — a New Natural Furocoumarin. Doklady Akad. Nauk S.S.S.R. 156, 1210 (1964); Chem. Abs. 61, 7000 (1964).

    Google Scholar 

  435. Nikonov, G. K.: Investigation of the Lactones of Monnier’s Cnidium (L.) Cuss. Zhur. obshchei Khim. 34, 1350 (1964); Chem. Abs. 61, 3352 (1964).

    Google Scholar 

  436. Nikonov, G. K.: Xanthogalin, a New Coumarin from Purple Xanthogalum (Xanthogalum pur- pur ascens Lallem. Zhur. obshchei Khim. 34, 3853 (1964); Chem. Abs. 62, 6454 (1965).

    Google Scholar 

  437. Nikonov, G. K.: A Study of Cnidimin and Its Identification with Libanotin. Khim. prirod. Soedinenii 4, 48 (1968); Chem. Abs. 69, 77062 (1968).

    Google Scholar 

  438. Nikonov, G. K.: Structure of the Coumarin Sachalinin. Khim. prirod. Soedinenii 6, 623 (1970); Chem. Abs. 76262 (1971).

    Google Scholar 

  439. Nikonov, G. K.: The Structure of Mogoltin, a Coumarin from the Roots of Peucedanum mogol- tavicum. Khim. prirod. Soedinenii 7, 572 (1971); Chem. Abs. 76, 59780 (1972).

    Google Scholar 

  440. Nikonov, G. K.: The Structure of Mogoltavin, a Coumarin from the Roots of Peucedanum mogol- tavicum. Khim. prirod. Soedinenii 8, 43 (1972); Chem. Abs. 77, 48653 (1972).

    Google Scholar 

  441. Nikonov, G. K.: The Structure of Mogoltavinin, a Coumarin from the Roots of Peucedanum mogol- tavicum. Khim. prirod. Soedinenii 8, 54 (1972); Chem. Abs. 77, 48647 (1972).

    Google Scholar 

  442. Nikonov, G. K., and D. I. Baranauskaite: Coumarins of Wormwood-Zosimia Zosimia absinthifolia (Vent.) Link. Zhur. obshchei Khim. 34, 3854 (1964); Chem. Abs. 62, 6465 (1965).

    Google Scholar 

  443. Nikonov, G. K., and D. I. Baranauskaite: Xanthogalin — a New Coumarin from Xanthogalum pur pur ascens Lallem. Khim. prirod. Soedinenii 1, 139 (1965); Chem. Abs. 63, 8303 (1965).

    Google Scholar 

  444. Nikonov, G. K., and D. I. Baranauskaite: Lactones of Zosimia absinthifolia (Vent) Link. Khim. prirod. Soedinenii 1, 220 (1965); Chem. Abs. 63, 13701 (1965).

    Google Scholar 

  445. Nikonov, G. K., and A. A. Ivashenko: The Chemical Structure of Morison’s Mountain Parsley Peucedanum morisonii Bess. Zhur. obshchei Khim. 33, 2740 (1963); Chem. Abs. 60, 1725 (1964).

    Google Scholar 

  446. Nikonov, G. K., and V. B. Kuvaev: The Lactone of Peucedanum mogoltavicum Korov. Zhur. obshchei Khim. 34, 1020 (1964); Chem. Abs. 60, 15820 (1964).

    Google Scholar 

  447. Nikonov, G. K., G. Y. Pek, and V. V. Vandyshev: The Structure of Agasyllin. Khim. prirod. Soedinenii 5, 119 (1969); Chem. Abs. 71, 61256 (1969).

    Google Scholar 

  448. Nikonov, G. K., and M. G. Pimenov: A Chemical Study of Angelica sachalinensis Maxim. Khim. prirod. Soedinenii 1, 73 (1965); Chem. Abs. 62, 16630 (1965).

    Google Scholar 

  449. Nikonov, G. K., and A. I. Saidkhodzhaev: The Structure of Pranferin, a New Coumarin from the Roots of Prangos ferulacea. Khim. prirod. Soedinenii 7, 255 (1971); Chem. Abs. 75, 110142 (1971).

    Google Scholar 

  450. Nikonov, G. K., R. K. Veremei, and M. G. Pimenov: (+)-5-(3’-Methyl-2’,3’- dihydroxy)-butoxypsoralen — a Natural Component of Angelica gmelini (D. C.) Wormsk. Ex Fisch. Zhur. obshchei Khim. 34, 1353 (1964); Chem. Abs. 61, 1821 (1964).

    Google Scholar 

  451. NovAk, I., Z. Rozsa, Y. W. Mirrhom, K. Szendrei, J. Reisch, and E. Minker: Isolation of Active Substances from Ruta Roots III. Marmesin, Marmesinin, Rutacultin and a Rutamarin Alcohol. Herba Hung. 11, 13 (1972); Chem. Abs. 79, 102812 (1973).

    Google Scholar 

  452. Ognyanov, I., and D. Bocheva: Natural Coumarins II. Felamidin (Benzoylmarmesin). Z. Naturforsch. 22b, 1231 (1967).

    CAS  Google Scholar 

  453. Ognyanov, I., and D. Bocheva: Pangeline and Angeloylpangeline. Two New Furocoumarins in the Roots of Angelica pancici. Doklady Bolg. Akad. Nauk 24, 315 (1971); Chem. Abs. 75, 45611 (1971).

    Google Scholar 

  454. Ognyanov, I., and D. Bocheva: Acid-Catalyzed Cleavage of Oxypeucedanin. Doklady Bolg. Akad. Nauk 25, 1061 (1972); Chem. Abs. 78, 58270 (1973).

    Google Scholar 

  455. Ovodov, Y. S., G. M. Frolova, M. Y. Nefedova, and G. B. Elyakov: Glycosides of Eleutherococcus senticocus II. The Structure of Eleutherosides A, Bi, C and D. Khim. prirod. Soedinenii 3, 63 (1967); Chem. Abs. 67, 54394 (1967).

    Google Scholar 

  456. Paknikar, S. K., and J. K. Kirtany: The Terpenoid Parts of Kamolone and Kamolol of Ferula penninervis. Experientia 30, 224 (1974).

    CAS  Google Scholar 

  457. Perel’son, M. E.: The Configuration of Polyanthin and Polyanthinin. Khim. prirod. Soedinenii 11, 249 (1975); Chem. Abs. 84, 5174 (1976).

    Google Scholar 

  458. Perel’son, M. E., A. I. Ban’kovskii, and N. E. Ermatov: A Study of the Structure and Configuration of the Terpenoid Coumarins Kamolol and Kamolone by PMR Spectroscopy with the addition of Eu(DPM)3. Khim. prirod. Soedinenii 11, 703 (1975); Chem. Abs. 84, 150766 (1976).

    Google Scholar 

  459. Perel’son, M. E., N. P. Kir’yalov, and A. I. Ban’kovskii: The Question of the Configurations of Farnesiferol A, Gummosin, Badrakemin, and Colladonin. Khim. prirod. Soedinenii 11, 244 (1975); Chem. Abs. 84, 5172 (1976).

    Google Scholar 

  460. Perel’son, M. E., A. A. Kir’yanov, A. I. Bankovskii, N. P. Kir’yalov, and T. V. Bukreeva: Studies of Stereochemistry of Terpenoidal Coumarins of the Iresane Series, Using the Method of Paramagnetic Resonance Spectroscopy with Eu(DPM)3 Additions. Khim. prirod. Soedinenii 12, 442 (1976); Chem. Abs. 86, 29944 (1977).

    Google Scholar 

  461. Perel’son, M. E., A. A. Kir’yanov, Y. E. Sklyar, and V. V. Vandyshev: Use of the Paramagnetic Shift Agent Eu(DPM)3 for Studying the Structure and Stereochemistry of Conferol and Conferone. Khim. prirod. Soedinenii 9, 726 (1973); Chem. Abs. 82, 16954 (1975).

    Google Scholar 

  462. Perel’son, M. E., Y. N. Sheinker, A. A. Savina, and G. P. Syrova: NMR Spectra of Natural Coumarin Derivatives III. Dihydrofurocoumarins and Dihydropyranocoumarins. Khim. prirod. Soedinenii 7,712 (1971); Chem. Abs. 76, 98583 (1972).

    Google Scholar 

  463. Perel’son, M. E., Y. N. Sheinker, and G. P. Syrova: NMR Spectra of Natural Coumarin Derivatives II. Furocoumarins. Khim. prirod. Soedinenii 7, 576 (1971); Chem. Abs. 76, 45335 (1972).

    Google Scholar 

  464. Perel’son, M. E., Y. N. Sheinker, G. P. Syrova, G. K. Nikonov, and A. P. Prokopenko: Use of NMR Spectroscopy in the Chemistry of Natural Coumarins. Trudy vses. nauch.-issled. Inst. Lek. Aromat. Rast. 15, 60 (1969); Chem. Abs. 75, 35617 (1971).

    Google Scholar 

  465. Perel’son, M. E., Y. N. Sheinker, G. P. Syrova, and K. F. Turchin: NMR Spectra of Natural Coumarin Derivatives I. Coumarins. Khim. prirod. Soedinenii 6, 6 (1970); Chem. Abs. 73, 34402 (1970).

    Google Scholar 

  466. Perel’son, M. E., V. V. Vandyshev, and Y. E. Sklyar: The Structure and Stereo­chemistry of Conferin. Khim. prirod. Soedinenii 11, 248 (1975); Chem. Abs. 84, 5173 (1976).

    Google Scholar 

  467. Perone, V. B.: The Natural Occurrence and Uses of the Toxic Coumarins. Microbial Toxins 8, 67 (1972).

    CAS  Google Scholar 

  468. Pfau, A. S.: Etudes sur les matières végétales volatiles, IX. Sur quelque constituants inédits de l’huile essentielle de rue. Helv. Chim. Acta 22, 382 (1939).

    Google Scholar 

  469. Pigulevskii, G. V., and G. A. Kuznetsova: Structure of a New Furocoumarin, Prangenine. Zhur. obshchei Khim. 23, 1237 (1953); Chem. Abs. 47, 12341 (1953).

    Google Scholar 

  470. Pigulevskii, G. V., and T. N. Naugol’naya: Resin from the Roots of Ferula gummosa. Trudy bot. Inst. Akad. Nauk S.S.R. 5, 80 (1955); Chem. Abs. 50, 15743 (1956).

    Google Scholar 

  471. Plouvier, V.: Recherche d’hétérosides coumariniques: le magnolioside du Magnolia macrophylla, le calycanthoside et le cichorioside des Fraxinus. Compt. rend. 266, D, 1526 (1968).

    Google Scholar 

  472. Plouvier, V.: Sur quelque constituants des écorces de Prunus mahaleb L. (Rosacées). Compt. rend. 250, 594 (1960).

    CAS  Google Scholar 

  473. Plouvier, V.: Sur deux hétérosides nouveaux, l’isofraxoside isolé du Diervilla lonicera Mill. (Caprifoliacées) et le poliothyroside isolé du Poliothyrsis sinensis Oliv. (Flacourtiacées). Compt. rend. 268, D, 1982 (1969).

    Google Scholar 

  474. Pousset, J. L., M. Debray, and R. R. Paris: Sur le Baissea leonensis, présence d’un nouvel hétéroside coumarinique, le baisseoside. Compt. rend. 271, D, 2320 (1970).

    Google Scholar 

  475. Pozzi, H., E. Sànchez, and J. Comin: Studies on Argentine Plants — XXII. Heliettin, a New Furocoumarin from Helietta longifoliata Britt. Tetrahedron 23, 1129 (1967).

    CAS  Google Scholar 

  476. Prokopenko, A. P.: Peucenidin — a New Furocoumarin Isolated from the Fruit of Mountain Peucedanum oreoselinum (L.) Moench. Zhur. obshchei Khim. 34, 4111 (1964); Chem. Abs. 62, 9117 (1965).

    Google Scholar 

  477. Prokopenko, A. P.: Libanotin, a New Furocoumarin from Libanotis transcaucasia Schischk. Khim. prirod. Soedinenii 1, 215 (1965); Chem. Abs. 63, 14638 (1965).

    Google Scholar 

  478. Prokopenko, A. P.: Coumarins of Libanotis intermedia. Rast Resursy 2, 201 (1966); Chem. Abs. 65, 12561 (1966).

    Google Scholar 

  479. Purushothaman, K. K., S. Vasanth, J. D. Connolly, and C. Labbé: 4,6,7- Trimethoxyl-5-methylchromen-2-one, a New Coumarin from Leonotis nepetaefolia. J. C. S. Perkin I 1976, 2594.

    Google Scholar 

  480. Raj, K., P. P. Joshi, D. S. Bhakuni, R. S. Kapil, and S. P. Popli: Synthesis of (i)-Auraptenol and Murrayone. Indian J. Chem. 14B, 332 (1976).

    Google Scholar 

  481. Raj, K., R. S. Kapil, and S. P. Popli: Synthesis of Subernol and Coumarin Rr8. Indian J. Chem. 13, 1404 (1975).

    Google Scholar 

  482. Rajendran, K., C. K. Mesta, S. K. Paknikar, and S. C. Bhattacharyya: Vaginol, a New Coumarin Related to Archangelicin. Indian J. Chem. 8, 200 (1970).

    CAS  Google Scholar 

  483. Ramstad, E., W. C. Lin, T. Lin, and W. Koo: Coumurrayin, A New Coumarin from Murraya paniculata ( L.) Jack. Tetrahedron Letters 1968, 811.

    Google Scholar 

  484. Reisch, J., S. A. Khaled, K. Szendrei, and I. Novàk: 5-Alkoxyfuranocoumarins from Peucedanum ostruthium. Phytochemistry 14, 1889 (1975).

    CAS  Google Scholar 

  485. Reisch, J., I. Novàk, K. Szendrei, and E. Minker: Rutamarin, ein Coumarin- Derivat aus Ruta graveolens. Acta Pharm. Suecica 4, 179 (1967); Chem. Abs. 67, 54057 (1967).

    Google Scholar 

  486. Reisch, J., I. Novàk, K. Szendrei, and E. Minker: Die Anwendung der KMR-Spektroskopie zur Strukturermittlung von Cumarin-Derivaten. Die Pharmazie 22, 205 (1967).

    CAS  Google Scholar 

  487. Reisch, J., and K. Szendrei: Photoisomerisierung des Chalepensin zum Rutolid (Clausindin). Arch. Pharm. (Weinheim) 308, 983 (1975).

    CAS  Google Scholar 

  488. Reisch, J., K. Szendrei, E. Minker, and I. Noväk: 3-(l’,1’-Dimethylallyl)-6-(3’,3’- dimethylallyl) umbelliferone (gravelliferon) aus den Wurzeln von Ruta graveolens. Experientia 24, 992 (1968).

    CAS  Google Scholar 

  489. Reisch, J., K. Szendrei, E. Minker, and I. Noväk: Chalepensin, Gravelliferon-Methyläther und 3-(1’,1’-Dimethylallyl)- herniarin aus den Wurzeln von Ruta graveolens. Tetrahedron Letters 1968, 4395.

    Google Scholar 

  490. Reisch, J., K. Szendrei, E. Minker, and I. Noväk: Neue C3-substituierte Cumarin-Derivate aus Ruta graveolens L.: 3-(1’,1’- Dimethylallyl)-daphnetindimethyläther, 8-Methoxygravelliferon, 3-(1’,1’-Dimethyl- allyl)-8-(3”3”-dimethylallyl)-xanthyletin. Tetrahedron Letters 1970, 4305.

    Google Scholar 

  491. Reisch, J., K. Szendrei, I. Noväk, and E. Minker: Suberenon, a New Coumarin Derivative from the Root of Ruta graveolens L. Magyar Kern. Folyöirat 78, 6 (1972); Chem. Abs. 76, 138149 (1972).

    Google Scholar 

  492. Reisch, J., K. Szendrei, Z. Rözsa, I. Noväk, and E. Minker: Rutacultin und Rutamarin-Alkohol aus den Wurzeln von Ruta graveolens. Phytochemistry 11, 1529 (1972).

    CAS  Google Scholar 

  493. Reyes, R. E., and A. G. Gonzäles: Quimica de las Rutaceas IV. Cumarinas de las hojas de la Ruta pinnata L. Fil: estructura de una nueva furocumarina. Anales de Quirn. 61, 803 (1965).

    CAS  Google Scholar 

  494. Reyes, R. E., and A. G. Gonzäles: Structure of Pinnarin and Furopinnarin, Two New Coumarins from Roots of Ruta pinnata. Phytochemistry 9, 833 (1970).

    Google Scholar 

  495. Reyes, R. E., and A. G. Gonzäles: Nuevas fuentes de cumarinas naturales XV. Estructura de la sabandinina, una nueva cumarina de la Ruta pinnata L. fil. Anales de Quím. 67, 207 (1971).

    Google Scholar 

  496. Reyes, R. E., and A. G. Gonzäles: Química de las Rutaceas IV. Cumarinas de las hojas de la Ruta pinnata L. fil; estructura de una nueva furocumarina. Farmacia Nueva 37, 729 (1972); Chem. Abs. 79, 9814 (1973).

    Google Scholar 

  497. Rodighiero, P., A. Guiotto, P. Manzini, and G. Pastorini: Synthesis of Ponci- marin, a New Coumarin from Poncirus trifoliata L. Z. Naturforsch. 30B, 987 (1975).

    Google Scholar 

  498. Rondest, J., B. C. Das, M.-N. Ricroch, C. Kan-Fan, R. Potier, and J. Polonsky: Plantes Malgaches-III. Etude des constituants de Evodia beiahe Bâillon (Rutacées). Phytochemistry 7, 1019 (1968).

    CAS  Google Scholar 

  499. Rybalko, K. S., O. A. Konovalova, V. I. Sheichenko, and P. I. Zakharov: Armin a New Coumarin from Artemisia armeniaca. Khim. prirod. Soedinenii 12, 294 (1976).

    Google Scholar 

  500. Saha, S. K., and A. Chatterjee: Isolation of Allo-imperatorin and β-sitosterol from the Fruits of Aegle marmelos Correa. J. Indian Chem. Soc. 34, 228 (1957).

    CAS  Google Scholar 

  501. Saidkhodzhaev, A. I., and G. K. Nikonov: The Configuration of Badrakemin and Gummosin, and the Identity of Isobadrakemin, Colladonin and Farnesiferol A. Khim. prirod. Soedinenii 9, 490 (1973); Chem. Abs. 80, 60048 (1974).

    Google Scholar 

  502. Saidkhodzhaev, A. I., and G. K. Nikonov: Confirmation of the Configurations of Badrakemin and Gummosin. Khim. prirod. Soedinenii 10, 15 (1974); Chem. Abs. 80, 121140 (1974).

    Google Scholar 

  503. Saiki, Y., K. Morinaga, O. Okegawa, S. Sakai, Y. Amaya, A. Ueno, and S. Fukushima: On the Coumarins of the Roots of Angelica dahurica Benth. et Hook. Yakugaku Zasshi 91, 1313 (1971); Chem. Abs. 76, 56621 (1972).

    Google Scholar 

  504. Saiki, Y., M. Uchida, O. Okegawa, and S. Fukushima: On the Mass Spectra of Several Furanocoumarins Having Various Isoprenoidal Residues. Chem. and Pharm. Bull. (Japan) 22, 1227 (1974).

    CAS  Google Scholar 

  505. Sano, K., I. Yosioka, and I. Kitagawa: Stereostructures of Decursin, Decursidin and a New Coumarin Isolated from Angelica decursiva. Chem. and Pharm. Bull. (Japan) 21, 2095 (1973).

    CAS  Google Scholar 

  506. Sano, K., I. Yosioka, and I. Kitagawa: Stereostructures of Decursin, Decursidin and Other New Pyranocoumarin Derivatives from the Root of Angelica decursiva. Chem. and Pharm. Bull. (Japan) 23, 20 (1975).

    CAS  Google Scholar 

  507. Savina, A. A., G. K. Nikonov, and A. I. Ban’kovskii: Seseliflorin — a New Coumarin from Seseli sessiliflorum. Khim. prirod. Soedinenii 6, 522 (1970); Chem. Abs. 74, 50519 (1971).

    Google Scholar 

  508. Savina, A. A., G. K. Nikonov, and M. E. Perel’son: Smirniorin, a New Coumarin from the Roots of Smirniopsis aucheri. Khim. prirod. Soedinenii 5, 592 (1969); Chem. Abs. 73, 25337 (1970).

    Google Scholar 

  509. Savina, A. A., and M. E. Perel’son: The Configuration of the Acid Residue in the Molecules of Floroselin, Seselirin and Seseliflorin. Khim. prirod. Soedinenii 7, 831 (1971); Chem. Abs. 76, 71910 (1972).

    Google Scholar 

  510. Savina, A. A., M. E. Perel’son, and G. K. Nikonov: The Structure of Smirnioridin. Khim. prirod. Soedinenii 6, 185 (1970); Chem. Abs. 73, 87813 (1970).

    Google Scholar 

  511. Savina, A. A., M. E. Perel’son, G. K. Nikonov, and A. I. Ban’kovskii: Floroselin — a New Coumarin from the Roots of Seseli sessiliflorum. Khim. prirod. Soedinenii 6, 517 (1970); Chem. Abs. 74, 84002 (1971).

    Google Scholar 

  512. Savina, A. A., and M. G. Pimenov: Seseli sessiliflorum, a New Source of Coumarins and Chromones. Rast. Resursy 8, 361 (1972); Chem. Abs. 77, 149719 (1972).

    Google Scholar 

  513. Savina, A. A., V. V. Vandyshev, M. E. Perel’son, and M. G. Pimenov: Edultin from Libanotis seseloides. Khim. prirod. Soedinenii 7, 116 (1971); Chem. Abs. 75, 16129 (1971).

    Google Scholar 

  514. Scheel, L. D., V. B. Perone, R. L. Larkin, and R. E. Kupel: The Isolation and Characterization of Two Phototoxic Furanocoumarins (Psoralens) from Diseased Celery. Biochemistry 2, 127 (1963).

    Google Scholar 

  515. Schneider, G., and H. Müller: Über das Furocumaringlucosid, Rutarin, aus der Weinraute. Arch. Pharm. 300, 913 (1967).

    CAS  Google Scholar 

  516. Schneider, G., H. Müller, and P. Pfaender: Rutaretin, ein neues Furocumarin aus Ruta graveolens L. Arch. Pharm. 300, 73 (1967).

    CAS  Google Scholar 

  517. Schönberg, A., and G. Aziz: Furo-chromones and -coumarins (X): On the Constitution of Prangenin. J. Amer. Chem. Soc. 77, 2563 (1955).

    Google Scholar 

  518. Schroeder, H. D., W. Bencze, O. Halpern, and H. Schmid: Struktur der Visnagane; Synthese von (±)-trans-Samidin. Chem. Ber. 92, 2338 (1959).

    CAS  Google Scholar 

  519. Seshadri, T. R., and M. S. Sood: Synthesis of Sphondin. J. Indian Chem. Soc. 39, 539 (1962).

    CAS  Google Scholar 

  520. Seshadri, T. R., and M. S. Sood: New Synthesis of Linear Furanocoumarins: Psoralen, Xanthotoxin and 8-Acetylpsoralen. Indian J. Chem. 1, 291 (1963).

    CAS  Google Scholar 

  521. Seshadri, T. R., and M. S. Sood: Chemical Comparison of the Roots of Selinum vaginatum and Nardostachys jatamansi. Phytochemistry 6, 445 (1967).

    CAS  Google Scholar 

  522. Seshadri, T. R., and M. S. Sood: Absolute Configuration of Selinidin, Vaginidin and Related Compounds. Current Sci. 36, 563 (1967).

    CAS  Google Scholar 

  523. Seshadri, T. R., M. S. Sood, K. L. Handa, and Vishwapaul: Constitution of Selinidin: a New Coumarin from Selinum vaginatum Clarke. Tetrahedron Letters 1964, 3367.

    Google Scholar 

  524. Seshadri, T. R., M. S. Sood, K. L. Handa, and Vishwapaul: Chemical Components of the Roots of Selinum vaginatum — I. Coumarins of the Petroleum Ether Extract. Tetrahedron 23, 1883 (1967).

    CAS  Google Scholar 

  525. Seshadri, T. R., and Vishwapaul: Sesibiricin, a New Coumarin from Seseli sibiricum. Indian J. Chem. b, 202 (1970).

    Google Scholar 

  526. Seshadri, T. R., and Vishwapaul: Chemical Components of the Roots of Selinum vaginatum — II. Chemistry of Vaginidin and Vaginidiol. Indian J. Chem. 9, 418 (1971).

    CAS  Google Scholar 

  527. Seshadri, T. R., and Vishwapaul: Recent Advances in Naturally Occurring Coumarins. J. Sci. Ind. Res., India 32, 227 (1973).

    CAS  Google Scholar 

  528. Shagova, L. I., V. N. Florya, G. A. Kuznetsova, and M. E. Perel’son: Diesters of Khellactone and Rutarin (Campesenin) from Seseli campestre growing in Moldavia. Khim. prirod. Soedinenii 9, 665 (1973).

    Google Scholar 

  529. Shanbhag, S. N., C. K. Mesta, M. L. Maheshwari, and S. C. Bhattacharyya: Terpenoids — LXXV. Constituents of Nardostachys jatamansi and Synthesis of (±)-Dihydrosamidin and Visnadin from Jatamansin. Tetrahedron 21, 3591 (1965).

    CAS  Google Scholar 

  530. Shanbhag, S. N., C. K. Mesta, M. L. Maheshwari, S. K. Paknikar, and S. C. Bhattacharyya: Terpenoids — LU. Jatamansin, a New Terpenic Coumarin from Nardostachys jatamansi. Tetrahedron 20, 2605 (1964).

    CAS  Google Scholar 

  531. Sharma, Y. N., R. C. Sharma, A. Zaman, and A. R. Kidwai: Chemical Examina­tion of Heracleum candicans II. Isolation and Structure of a New Furocoumarin, Heraclenol. Naturwiss. 51, 537 (1964).

    CAS  Google Scholar 

  532. Sharma, Y. N., A. Zaman, and A. R. Kidwai: Chemical Examination of Heracleum candicans — I. Isolation and Structure of a New Furocoumarin — Heraclenin. Tetrahedron 20, 87 (1964).

    CAS  Google Scholar 

  533. Sharma, Y. N., A. Zaman, A. R. Kidwai, R. B. Bates, and V. P. Thalacker: Coumarin Constituents of Heracleum candicans — III. Tetrahedron 22, 3221 (1966).

    CAS  Google Scholar 

  534. Sheichenko, V. I., and V. V. Vandyshev: The Composition of Visnadin. Khim. prirod. Soedinenii 7, 368 (1971); Chem. Abs. 75, 110204 (1971).

    Google Scholar 

  535. Sheinker, Y. N., G. K. Nikonov, M. E. Perel’son, G. P. Syrova, G. Y. Pek, N. S. Vul’fson, V. I. Zaretskii, and V. G. Zaikin: Structure of Peucenol (Peumorisin) a New Hydroxycoumarin. Khim. prirod. Soedninenii 5, 361 (1969); Chem. Abs. 72, 66744 (1970).

    Google Scholar 

  536. Shipchandler, M., and T. O. Soine: A Revised Structure of Columbianin and Pertinent Mass Spectral Studies. J. Pharm. Sci. 57, 747 (1968).

    CAS  Google Scholar 

  537. Shipchandler, M., T. O. Soine, and P. K. Gupta: Coumarins XI: A Total Synthesis of (±)-Columbianetin. J. Pharm. Sci. 59, 67 (1970).

    CAS  Google Scholar 

  538. Sklyar, Y. E., L. G. Avramenko, and L. I. Dukhovlinova: A Method of Obtain­ing Felamidin. Khim. prirod. Soedinenii 9, 427 (1973); Chem. Abs. 79, 78647 (1973).

    Google Scholar 

  539. Sklyar, Y. E., M. E. Perel’son, and M. G. Pimenov: Moschatol, a New Coumarin from the Roots of Ferula moschata. Khim. prirod. Soedinenii 9, 428 (1973); Chem. Abs. 79, 102791 (1973).

    Google Scholar 

  540. Smith, E., N. Hosansky, and W. G. Bywater: Constitution of Samidin, Dihydro- samidin and Visnadin. Chem. and Ind. 1956, 718.

    Google Scholar 

  541. Smith, E., N. Hosansky, W. G. Bywater, and E. E. Van Tamelen: Constitution of Samidin, Dihydrosamidin and Visnadin. J. Amer. Chem. Soc. 79, 3534 (1957).

    Google Scholar 

  542. Smith, E., L. A. Pucchi, and W. G. Bywater: Crystalline Visnagan. Science 115, 520 (1952).

    CAS  Google Scholar 

  543. Soine, T.: Naturally Occurring Coumarins and Related Physiological Activities. J. Pharm. Sci. 53, 231 (1964).

    CAS  Google Scholar 

  544. Soine, T. O., and F. H. Ja wad: Structure of Lomatin, a New Coumarin. J. Pharm. Sci. 53, 990 (1964).

    CAS  Google Scholar 

  545. Soine, T. O., A. Zheleva, M. M. Mahandru, P. Erhardt, and L. Bubeva-Ivanova: Natural Coumarins VII: Isolation and Structure of a New Coumarin, Peuruthenicin, from Peucedanum ruthenicum M. B. J. Pharm. Sci. 62, 1879 (1973).

    CAS  Google Scholar 

  546. Sokolova, A. I., and G. K. Nikonov: Structure of Xanthalin. Khim. prirod. Soedinenii 6, 14 (1970); Chem. Abs. 73, 35157 (1970).

    Google Scholar 

  547. Sokolova, A. I., G. K. Nikonov, M. E. Perel’son, G. P. Syrova, and Y. N. Sheinker: The Structure of Xanthaline. Khim. prirod. Soedinenii 4, 280 (1968); Chem. Abs. 70, 77713 (1969).

    Google Scholar 

  548. Sokolova, A. I., M. E. Perel’son, and G. K. Nikonov: Tomasin, a New Coumarin from Xanthogalum purpurascens. Khim. prirod. Soedinenii 5, 359 (1969); Chem. Abs. 72, 97296 (1970).

    Google Scholar 

  549. Sokolova, A. I., Y. E. Sklyar, M. E. Perel’son, and M. G. Pimenov: Furocoumarins of Komarovia anisospermum. Khim. prirod. Soedinenii 12, 166 (1976); Chem. Abs. 85, 59598 (1976).

    Google Scholar 

  550. Stanley, W. L., and L. Jurd: Citrus Coumarins. Agric. Food Chem. 19, 1106 (1971).

    CAS  Google Scholar 

  551. Stanley, W. L., and S. H. Vannier: Chemical Composition of Lemon Oil. I. Isolation of a Series of Substituted Coumarins. J. Amer. Chem. Soc. 79, 3488 (1957).

    CAS  Google Scholar 

  552. Stanley, W. L., A. C. Waiss, R. E. Lundin, and S. H. Vannier: Auraptenol, a Coumarin Compound in Bitter (Seville) Orange Oil. Tetrahedron 21, 89 (1965).

    CAS  Google Scholar 

  553. Starkowsky, N. A., and N. Badran: Ammajin, a New Constituent of Ammi majus L. J. Org. Chem. 23, 1818 (1958).

    CAS  Google Scholar 

  554. Steck, W.: New Synthesis of Columbianetin and Related Coumarins. Canad. J. Chem. 49, 1197 (1971).

    CAS  Google Scholar 

  555. Steck, W.: New Syntheses of Demethylsuberosin, Xanthyletin, (i)-Decursinol, (+)-Marmesin, (-)-Nodakenetin, (±)-Decursin, and (±)-Prantschimgin. Canad. J. Chem. 49, 2297 (1971).

    CAS  Google Scholar 

  556. Steck, W.: Paniculatin, a New Coumarin from Murraya paniculata (L.) Jack. Canad. J. Chem. 50, 443 (1972).

    CAS  Google Scholar 

  557. Steck, W.: Coumarins and Chromones from Lomatium macrocarpum. Phytochemistry 12, 2283 (1973).

    Google Scholar 

  558. Steck, W., and B. K. Bailey: Leaf Coumarins of Angelica archangelica. Canad. J. Chem. 47, 2425 (1969).

    CAS  Google Scholar 

  559. Characterization of Plant Coumarins by Combined Gas Chromatography, Ultraviolet Absorption Spectroscopy, and Nuclear Magnetic Resonance Analysis. Canad. J. Chem. 47, 3577 (1969).

    Google Scholar 

  560. Steck, W., B. K. Bailey, J. P. Shyluk, and O. L. Gamborg: Coumarins and Alkaloids from Cell Cultures of Ruta graveolens. Phytochemistry 10, 191 (1971).

    CAS  Google Scholar 

  561. Steck, W., and S. A. Brown: Biosynthesis of Angular Furanocoumarins. Canad. J. Biochem. 48, 872 (1970).

    CAS  Google Scholar 

  562. Steck, W., and S. A. Brown: Comparison of (+)- and (—)-Marmesin as Intermediates in the Biosynthesis of Linear Furanocoumarins. Canad. J. Biochem. 49, 1213 (1971).

    CAS  Google Scholar 

  563. Steck, W., and M. Mazurek: Identification of Natural Coumarins by Nmr Spectroscopy. Lloydia 35, 418 (1972).

    CAS  Google Scholar 

  564. Steck, W., and L. R. Wetter: Apterin, an Unusual Glucoside of Zizia aptera. Phytochemistry 13, 1925 (1974).

    CAS  Google Scholar 

  565. Stemple, N. F., and W. H. Watson: The Crystal and Molecular Structure of Xanthotoxin, C12H18O4. Acta Cryst. 28B, 2485 (1972).

    CAS  Google Scholar 

  566. Stermitz, F. R., and R. D. Thomas: Separation of Furocoumarins by High- Pressure Liquid Chromatography. J. Chromat. 77, 431 (1973).

    CAS  Google Scholar 

  567. Stout, G. H., and K. L. Stevens: The Structure of Costatolide. J. Org. Chem. 29, 3604 (1964).

    CAS  Google Scholar 

  568. Svendsen, A. B.: Zur Chemie norwegischer Umbelliferen. Diss. University Oslo 1954; Chem. Abs. 52, 2173 (1958).

    Google Scholar 

  569. Szendrei, K., E. Minker, I. Noväk, and J. Reisch: Biosynthesis of Rutaceae Components. Herba Hung. 9, 33 (1970); Chem. Abs. 75, 95445 (1971).

    Google Scholar 

  570. Szendrei, K., M. Petz, I. Novàk, J. Reisch, H. E. Bailey, and V. L. Bailey: Isolation and Structure Analysis of Quinoline Alkaloids and Coumarins from Ptelea tr if oliata subspecies pallida var. confinis. Herb. Hung. 13, 49 (1974); Chem. Abs. 83, 40169 (1975).

    Google Scholar 

  571. Talapatra, B., S. K. Mukhopadhyay, M. K. Chaudhuri, and S. K. Talapatra: Synthesis of 6,7-Dihydro-8,8-dimethyl-2H,8H-benzo[l,2-6:5,4-6’]-dipyran-2,6-dione (Graveolone): An Unusual Bromination of Dihydroxanthyletin by N-Bromosuccini- mide in Presence of Lead Tetraacetate. Indian J. Chem. 14B, 129 (1976).

    Google Scholar 

  572. Talapatra, S. K., M. Bhattacharyya, B. Talapatra, and B. C. Das: Xylotenin, a New Furocoumarin from Chloroxylon swietenia DC. J. Indian Chem. Soc. 45, 861 (1968).

    CAS  Google Scholar 

  573. Talapatra, S. K., L. N. Dutta, and B. Talapatra: The Structure and Stereo­chemistry of Murrangatin. A New Monomeric Coumarin from Murraya elongata Alph. DC. Tetrahedron 29, 2811 (1973).

    CAS  Google Scholar 

  574. Talapatra, S. K., L. N. Dutta, and B. Talapatra: Structure of Murralongin, a Novel Monomeric Coumarin from Murraya elongata: Stereochemistry and Preferred Conformation of its Unique Side Chain. Tetrahedron Letters 1973, 5005.

    Google Scholar 

  575. Talapatra, S. K., S. K. Mukhopadhyay, and B. Talapatra: Nodakenetin Acetate: A New Coumarin from Boenninghausenia albiflora. Phytochemistry 12, 2312 (1973).

    CAS  Google Scholar 

  576. Talapatra, S. K., L. N. Dutta, and B. Talapatra: Minor Coumarins of Boenninghausenia albiflora. Phytochemistry 14, 836 (1975).

    CAS  Google Scholar 

  577. Tanino, H., and S. Inoue: Synthesis of Coumurrayin. Chem. and Pharm. Bull. (Japan) 17, 1071 (1969).

    CAS  Google Scholar 

  578. Terazawa, M., and T. Sasaya: Extractives of Yachidamo, Fraxinus mandshurica var. japónica. II. Glucosides in bark. Mokuzai Gakkaishi 16, 192 (1970); Chem. Abs. 74, 108116 (1971).

    Google Scholar 

  579. Tomimatsu, T., H. Hasegawa, and K. Tori: Studies on the Chemical Components of the Rutaceae Plants — VII. Components of the Roots of Poncirus tri/oliata Rafinesque (5). Poncitrin, a New Coumarin: Structure and Chemical Degradation. Tetrahedron 30, 939 (1974).

    CAS  Google Scholar 

  580. Tomimatsu, T., M. Hashimoto, T. Shingu, and K. Tori: Poncitrin, a New Coumarin: Structure and Nuclear Overhauser Effects. J. Chem. Soc. (D) 1969, 168.

    Google Scholar 

  581. Tomimatsu, T., M. Hashimoto, T. Shingu, and K. Tori: Studies on the Chemical Components of Rutaceae Plants — VI. Components of the Root of Poncirus trifoliata Rafinesque (4). Poncitrin, a New Coumarin: Structure and Nuclear Overhauser Effects. Tetrahedron 28, 2003 (1972).

    Google Scholar 

  582. Turabelidze, D. G., G. K. Nikonov, and E. P. Kemgrtelidze: Coumarins of the Roots of Libanotis transcaucasica. Khim. prirod. Soedinenii 10, 402 (1974); Chem. Abs. 81, 117102 (1974).

    Google Scholar 

  583. Vandyshev, V. V., G. K. Nikonov, and M. G. Pimenov: Coumarins of Agasyllis latifolia. Rast Resursy 4, 330 (1968); Chem. Abs. 70, 17563 (1969).

    Google Scholar 

  584. Vandyshev, V. V., M. E. Perel’son, Y. E. Sklyar, and M. D. Moroz: Conferin — New Coumarin from the Roots of Ferula conocaula. Khim. prirod. Soedinenii 10, 660 (1974); Chem. Abs. 82, 73218 (1975).

    Google Scholar 

  585. Vandyshev, V. V., Y. E. Sklyar, M. E. Perel’son, and M. D. Moroz: Conferdione — a New Coumarin from Ferula conocaula. Khim. prirod. Soedinenii 10, 658 (1974); Chem. Abs. 82, 73217 (1975).

    Google Scholar 

  586. Vandyshev, V. V., Y. E. Sklyar, M. E. Perel’son, M. D. Moroz, and M. G. Pimenov: Conferone, a New Terpenoid Coumarin from the Fruit of Ferula conocaula. Khim. prirod. Soedinenii 8, 669 (1972); Chem. Abs. 78, 108266 (1973).

    Google Scholar 

  587. Vandyshev, V. V., Y. E. Sklyar, M. E. Perel’son, M. D. Moroz, and M. G. Pimenov: Conferol, a New Coumarin from the Roots of Ferula conocaula and F. moschata. Khim. prirod. Soedinenii 8, 670 (1972); Chem. Abs. 78, 108265 (1973).

    Google Scholar 

  588. Van Sumere, C. F., G. Wolf, H. Teuchy, and J. Kint: A New Thin-Layer Method for Phenolic Substances and Coumarins. J. Chromat. 20, 48 (1965).

    Google Scholar 

  589. Van Tamelen, E. E., and R. M. Coates: Biogenetic-Type Synthesis of (±)-Farnesiferol A and (±)-Farnesiferol C. Chem. Comm. 1966, 413.

    Google Scholar 

  590. Varga, E., K. Szendrei, I. Novák, and J. Reisch: Isolation of Coumarin Glyco­sides from Tissue Cultures of Ruta graveolens. Acta Pharm. Hung. 44, Suppl. 36 (1974); Chem. Abs. 82, 13996 (1975).

    Google Scholar 

  591. Venturella, P., A. Bellino, and F. Piozzi: Coumarin from Ekebergia senegalensis. Revision. Heterocycles 2, 345 (1974).

    CAS  Google Scholar 

  592. Venturella, P., A. Bellino, and F. Piozzi: Revised Structure for Siderin. Tetrahedron Letters 1974, 979.

    Google Scholar 

  593. Von Brocke, W., E. Reinhard, G. Nicholson, and W. A. König: Über das Vor­kommen von 3-(1’,1’-Dimethylallyl)-scopoletin in Gewebekulturen von Ruta graveolens. Z. Naturforsch. 26B, 1252 (1971).

    Google Scholar 

  594. Wagner, H., and S. Bladt: Cumarine aus südafrikanischen Pelargonium-Arten. Phytochemistry 14, 2061 (1975).

    CAS  Google Scholar 

  595. Wagner, H., S. Bladt, D. J. Abraham, and H. Lotter: Neue Cumarine aus Pelar­gonium reniforme Curt-Wurzel. Tetrahedron Letters 1974, 3807.

    Google Scholar 

  596. Wessely, F., and E. Demmer: Konstitution und Eigenschaften des Fraxins. Ber. 62, 120 (1929).

    Google Scholar 

  597. Willette, R. E., and T. O. Soine: Coumarins I. Isolation, Purification and Structure Determination of Pteryxin and Suksdorfin. J. Pharm. Sci. 51, 149 (1962).

    CAS  Google Scholar 

  598. Coumarins II. Structure of Columbianadin and Columbianin. J. Pharm. Sci. 53, 275 (1964).

    Google Scholar 

  599. Worden, L. R., K. D. Kaufman, J. A. Weis, and T. K. Schaaf: Synthetic Furo- coumarins. IX. A New Synthetic Route to Psoralen. J. Org. Chem. 34, 2311 (1969).

    CAS  Google Scholar 

  600. Yamada, S., N. Oh-Hashi, and K. Achiwa: Synthetic Studies on Optically Active Epoxyterpenes from L-Glutamic Acid — I. Syntheses of R-(+)-Epoxygeraniol, R-(+)- of Marmin and R-(+)-Epoxyaurapten. Tetrahedron Letters 1976, 2557.

    Google Scholar 

  601. Yamada, Y., C.-S. Hsu, K. Iguchi, M. Suzuki, H.-Y. Hsu, and Y.-P. Chen: Two New Khellactone Esters from Peucedanum japonicum Thunb. Tetrahedron Letters 1974, 2513.

    Google Scholar 

  602. Yamamoto, K., H. Irie, and S. Uyeo: Studies on the Constituents of the Rhizomes of Glaucidium palmatum II. The Total Synthesis of Glaupalol. Yakugaku Zasshi 91, 257 (1971); Chem. Abs. 74, 125509 (1971).

    Google Scholar 

  603. Yusupov, M. I., and G. P. Sidyakin: A Hydroxycoumarin Arscotin from Artemisia scotina. Khim. prirod. Soedinenii 9, 430 (1973).

    CAS  Google Scholar 

  604. Yusupov, M. I., and G. P. Sidyakin: Fraxidin and Isofraxidin from Artemisia scotina. Khim. prirod. Soedinenii 11, 91 (1975); Chem. Abs. 83, 128637 (1975).

    Google Scholar 

  605. Zakharov, P. I., V. S. Kabanov, A. I. Ban’kovskii, G. K. Nikonov, and N. E. Ermatov: A Mass Spectrometric Study of Some Dihydropyranocoumarins. Khim. prirod. Soedinenii 7, 398 (1971); Chem. Abs. 75, 139893 (1971).

    Google Scholar 

  606. Zakharov, P. I., V. S. Kabanov, M. E. Perel’son, A. I. Ban’kovskii, and N. E. Ermatov: Study of Natural Coumarins by Mass Spectroscopy I. Mass Spectra of Kamolone and Kamolol. Khim. prirod. Soedinenii 6, 296 (1970); Chem. Abs. 73, 76374 (1970).

    Google Scholar 

  607. Zakharov, P. I., P. B. Terent’ev, G. K. Nikonov, and A. I. Ban’kovskii: A Mass- Spectrometric Study of 3’,4’-Dihydroxy- and 3’,4’-Diacycloxydihydropyranocouma- rins. Khim. prirod. Soedinenii 7, 704 (1971); Chem. Abs. 76, 125962 (1972).

    Google Scholar 

  608. Zakharov, P. I., P. B. Terent’ev, G. K. Nikonov, and A. I. Ban’kovskii: A Mass-Spectrometric Study of Angular and Linear Diacycloxydihydrofurocoumarins. Khim. prirod. Soedinenii 8, 275 (1972); Chem. Abs. 77, 151143 (1972).

    Google Scholar 

  609. Zakharov, P. I., P. B. Terent’ev, G. K. Nikonov, and A. I. Ban’kovskii: A Mass-Spectrometric Study of Linear Monohydroxy- and Monoacyloxydihydrofurocoumarins. Khim. prirod. Soednineii 8, 431 (1972); Chem. Abs. 78, 15097 (1973).

    Google Scholar 

  610. Zakharov, P. I., P. B. Terent’ev, G. K. Nikonov, and A. I. Ban’kovskii: Mass-Spectrometric Study of the Coumarins Mogoltin, Mogoltavin, and Mogoltavinin. Khim. prirod. Soedinenii 10, 18 (1974); Chem. Abs. 80, 121139 (1974).

    Google Scholar 

  611. Zakharov, P. I., P. B. Terent’ev, G. K. Nikonov, A. I. Ban’kovskii, N. D. Antonova, and A. P. Prokopenko: The Structure of Peucenidin. Khim. prirod. Soedinenii 8, 271 (1972); Chem. Abs. 77, 164558 (1972).

    Google Scholar 

  612. Zaretskii, V. I., N. S. Vul’fson, L. S. Chetverikova, and V. G. Zaitkin: Mass- Spectrometric Investigation of Heterocyclic Compounds. Structure of Peumorisin — a New Natural Hydroxycoumarin Isolated from Peucedanum morisonii (Bess.) Zhur. obshchei Khim. 34, 3655 (1964); Chem. Abs. 62, 9097 (1965).

    Google Scholar 

  613. Zheleva, A. B., L. Bubeva-Ivanova, and S. L. Spasov: On the Structure of Peuarenarine, a New Coumarin from Peucedanum arenarium. Z. Naturforsch. 26B, 113 (1971).

    CAS  Google Scholar 

  614. Zheleva, A. B., M. M. Mahandru, and L. Bubeva-Ivanova: Four New Coumarins from the Roots of Peucedanum arenarium. Phytochemistry 15, 209 (1976).

    CAS  Google Scholar 

  615. Zheleva, A. B., M. M. Mahandru, and L. Bubeva-Ivanova: Stereochemistry of Isokhellactone Derived Coumarins from Peucedanum arenarium. Phytochemistry 15, 1293 (1976).

    CAS  Google Scholar 

  616. Zheleva, A. B., T. O. Soine, and L. Bubeva-Ivanova: Natural Coumarins V. Isolation of Xanthalin and a New Pyranocoumarin Peuarenine from Peucedanum arenarium. J. Pharm. Sci. 61, 1643 (1972).

    CAS  Google Scholar 

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Murray, R.D.H. (1978). Naturally Occurring Plant Coumarins. In: Herz, W., Grisebach, H., Kirby, G.W. (eds) Fortschritte der Chemie Organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Fortschritte der Chemie Organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products, vol 35. Springer, Vienna. https://doi.org/10.1007/978-3-7091-8505-6_4

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