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Carbamate als Agrarchemikalien

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Angewandte Chemie

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Literatur

  1. Wettlauf mit der Resistenz. Hauptproblem der Schädlingsbekämpfung. Chem. Industrie 15, 13 (1963).

    Google Scholar 

  2. The Pesticide Situation for 1962–63 (Sept. 63) und The Pesticide Situation for 1964–65. U.S. Dep. of Agriculture, Sept. 1965.

    Google Scholar 

  3. Upward trend continues. Herbicides lead Increase in Pesticide Sales. Agric. Chemicals 20 (10), 46 (1965).

    Google Scholar 

  4. Shepard, H. H., and N. Mahan: Use of Agricultural Chemicals Continues to Rise. Chem. Engng. News 44 (36), 82 (1966).

    Google Scholar 

  5. Here's what they're saying about the 1966 Pesticide Season. Farm Chemicals 129 (10), 28 (1966).

    Google Scholar 

  6. Hanf, M.: Entwicklung und Ausmaß der Pflanzenschutzmittel-Anwendung. Z. Pflanzenkrankh. (Pflanzenpathol.) Pflanzenschutz 73 (9), 522 (1966).

    Google Scholar 

  7. Audus, L. J.: The Physiology and Biochemistry of Herbicides. London: Academic Press Inc. Ltd. 1964.

    Google Scholar 

  8. Sharvelle, E. G.: The Nature and Use of Modern Fungicides. Burgess Publishing Comp.(1961).

    Google Scholar 

  9. Metcalf, R. L.: Organic Insecticides. Their Chemistry and Mode of Action. New York: Interscience Publishers Inc. 1955.

    Google Scholar 

  10. Schrader, G.: Die Entwicklung neuer insektizider Phosphorsäureester. Weinheim/Bergstraße: Verlag Chemie 1963.

    Google Scholar 

  11. Friesen, G.: Untersuchungen über die Wirkung des Phenylurethans auf Samenkeimung und Entwicklung. Planta 8, 666 (1929).

    Article  CAS  Google Scholar 

  12. Templemann, W. G., and W. A. Sexton: Effect of Some Aryl-carbamic esters and Related Compounds upon Cereals and other Plant Species. Nature (London), 156, 630 (1945).

    Google Scholar 

  13. --Imperial Chemical Industries Limited, Brit. Patent 574995, 12.5.41, 30.1.46. DBP 833274, 23.10.48, 31.1.52.

    Google Scholar 

  14. George, D. K., D. H. Moore, W. P. Brian, and J. A. Garmann: Relative Herbicidal and Growth Modifying Activity of Several Esters of N-Phenylcarbamic acid. J. agric. Food Chem. 2, 356 (1954).

    Article  CAS  Google Scholar 

  15. De Rose, H. R.: Agronomy J. 43, 139 (1951).

    Article  Google Scholar 

  16. Witmann, E. D.: Pittsburgh Plate Glass Co., U.S. Patent 2695225, 21.5.54, 23.11.54.

    Google Scholar 

  17. Shaw, W. S., and C. R. Swanson: The Relation of Structural Configuration to the Herbicidal Properties and Phytotoxicity of Several Carbamates and other Chemicals. Weeds 2, 43 (1953).

    CAS  Google Scholar 

  18. Stefanye, D., and H. R. De Rose: Comparative Herbicidal Activities of Carbamates and N-Substituted Derivates. J. agric. Food Chem. 7, 425 (1959).

    Article  CAS  Google Scholar 

  19. Willard, J. R., u. K. P. Dorschner: F. M. C. Corp. DBP 1195549, 11.1.62, 24.6.65 (U.S. Priorität 24.1. 61).

    Google Scholar 

  20. Hopkins, T. R., J. County, and J. W. Pullen: Spencer Chemical Comp., U.S. Patent 2906614, 24.3.58, 29.9.59, DBP 1137255, 23.3.59, 27.9.62.

    Google Scholar 

  21. Fischer, A.: Neue Herbizide zur Unkrautbekämpfung in Rüben-und Gemüsekulturen im Vorauflaufverfahren. Z. Pflanzenkrankh. (Pflanzenpathol.) Pflanzenschutz 67, (10), 577 (1960).

    CAS  Google Scholar 

  22. -H. Windel u. H. Stummeyer: BASF A.G., DBP 1034 912, 24.7.58, 8.1.59.

    Google Scholar 

  23. Gysin, H., u. E. Knüsli: J. R. Geigy A.G., U.S. Patent 2 776196, 23.8.54, 1.1.57 (Schweizer Priorität 2.8.53).

    Google Scholar 

  24. Haubein, A. H.: Hercules Powder Comp., U.S. Patent 3 140167, 7.6.62, 7.7.64

    Google Scholar 

  25. Haubein, A. H. and J. R. Hansen: Some New Methylcarbamate Preemergence Crabgrass Herbicides. J. agric. Food Chem. 13, 555 (1965).

    Article  CAS  Google Scholar 

  26. Herrett, R. A., and R. V. Berthold: 3,4-Dichloro-benzylmethyl-carbamate and Related Compounds as Herbicides. Science (Washington) 149, 191 (1965).

    CAS  Google Scholar 

  27. Tolbert, N. E.: 2-Chloroethyl-trimethylammoniumchloride and Related Compounds on Plant Growth Substance. II. Effect on Growth of Wheat. Plant. Physiol. 35, 380 (1960).

    Article  CAS  Google Scholar 

  28. Krewson, Ch. F., J. W. Wood, W. C. Wolfe, J. W. Mitchell, and P. C. Marth: Synthesis and Biological Activity of Some Quaternary Ammonium and Related Compounds That Suppress Plant Growth. J. agric. Food Chem. 7, 264 (1959).

    Article  CAS  Google Scholar 

  29. Jung, J.: Versuchsergebnisse über die Wirkung von CCC bei Weizen. “CCC Research Symp.” Geneva, Switzerland. Techn. Dep. Cyanamid Int., Wayne/New Jersey.

    Google Scholar 

  30. Stedmann, E., and G. Barger: Physostigmine (Eserine). Part III. J. chem. Soc. (London) 127, 247 (1925).

    Google Scholar 

  31. Stevens, J. R., and R. H. Beutel: Physostigmine Substitutes. J. Amer. chem. Soc. 63. 308 (1941).

    Article  CAS  Google Scholar 

  32. Stedmann, E.: Studies on the Relationship between Chemical Constitution and Physiological Action. Biochem. J. 20, 719 (1926).

    Google Scholar 

  33. Kolbezen, M. J., R. L. Metcalf, and T. R. Fukuto: Insecticidal Activity of Carbamate Cholinesterase Inhibitors. J. agric. Food Chem. 2, 864 (1954).

    Article  CAS  Google Scholar 

  34. O'Brien, R. D., and R. W. Fisher: The Relation between Ionisation and Toxicity to Insects for Some Neuropharmacological Compounds. J. econ. Entomol. 51, 169 (1958).

    Google Scholar 

  35. Gysin, H.: über einige neue Insektizide. Chimia (Zürich) 8, 205 (1954).

    CAS  Google Scholar 

  36. Geigy, J. R., A.G.: Schweiz. Patent 279553, 22.8.49, 1.3.52, Schweiz. Patent 282655, 26.8.49, 15.5.52, Brit. Patent 681376, 23.11.49, 22.10.52.

    Google Scholar 

  37. Lambrech, J. A.: Union Carbide Corp.: U.S. Patent 2903478, 7.8.58, 8.9.59, U.S. Patent 3009855, 7.9.59, 21.11.61, D.B. Patent 1138277, 24.8.56, 18.10.62 (U.S. Priorität 29.8.55).

    Google Scholar 

  38. Haynes, H. L., J. A. Lambrech, and H. H. Moorefield: Insecticidal Properties and Characteristics of 1-Naphtyl-N-methylcarbamate. Contr. Boyce Thompson Inst. 18, 507 (1957).

    CAS  Google Scholar 

  39. Metcalf, R. L.: Carbamate Insecticides. Agric. Chemicals 16, (6), 20 (1961).

    CAS  Google Scholar 

  40. Bach, R. C.: Significant Developments in Eight Years with Sevin Insecticide. J. agric. Food Chem. 13, 198 (1965).

    Article  Google Scholar 

  41. Kilsheimer, J. R., u. H. H. Moorefield: Union Carbide Corp., DBP 1156273, 23.12.61, 24.10.63 (U.S. Priorität 30.12.60).

    Google Scholar 

  42. --Union Carbide Corp., DBP 1181979, 23.12.61, 19.11.64 (U.S. Priorität 30.12.60).

    Google Scholar 

  43. Fukuto, T. R.: The Chemistry of Organic Insecticides. Annu. Rev. Entomol. 6, 324 (1961).

    Article  Google Scholar 

  44. Kohn, G. K., J. N. Ospenson, and J. E. Moore: Some Structural Relationships of a Group of Simple Alkyl Phenyl N-Methylcarbamates to Anticholinesterase Activity. J. agric. Food Chem. 13, 232 (1965).

    Article  CAS  Google Scholar 

  45. Czyzewski, A., u. A. Jäger: Schering A.G., DBP 1156272, 7.5.60, 24.10.63.

    Google Scholar 

  46. Lemin, A. J.: The Upjohn Comp., U.S. Pat. 3131215, 6.10.60, 28.4.64.

    Google Scholar 

  47. -, G. A. Boyack, and R. M. Mac Donald: Alkyl and Halophenyl-N-Methylcarbamates. J. agric. Food Chem. 13, 214 (1965).

    Article  CAS  Google Scholar 

  48. Böcher, E., D. Delfs, G. Unterstenhöfer u. W. Behrenz: Farbenfabriken Bayer A.G., DBP 1108202, 31.7.59, 28.12.61.

    Google Scholar 

  49. Metcalf, R. L., T. R. Fukuto, and M. Y. Winton: Alkoxyphenyl N-Methylcarbamates as Insecticides. J. econ. Entomol. 53, 828, (1960).

    CAS  Google Scholar 

  50. --, M. Frederickson, and L. Peak: Insecticidal Activity of Alkylthiophenyl N-Methylcarbamates. J. agric. Food Chem. 13, 473 (1965).

    Article  Google Scholar 

  51. Schrader, G.: Zur Kenntnis neuer, wenig toxischer Insektizide auf der Basis von Phosphorsäureestern. Angew. Chem. 73, 331 (1961).

    CAS  Google Scholar 

  52. Hammann, I., R. HeiΒ, E. Schegk, G. Schrader u. K. Wedemeyer: Farbenfabriken Bayer A.G., DBP 1148107, 2.6.61, 2.5.63.

    Google Scholar 

  53. Metcalf, R. L., T. R. Fukuto, and M. Frederickson: Para-Substituted Meta-Xylenyl-Diethyl Phosphates and N-Methylcarbamates as Anticholinesterases and Insecticides. J. agric. Food Chem. 12, 231 (1964).

    Article  CAS  Google Scholar 

  54. Shulgin, A. T.: The Dow Chemical Comp., U.S. Pat. 3084098, 4.11.59, 2.4.63. DBP 1181978, 16.9.60, 19.11.64.

    Google Scholar 

  55. HeiΒ, R., E. Böcker u. G. Unterstenhöfer: Farbenfabriken Bayer A.G., DBP 1145162,20.7.60, 17.10.63.

    Google Scholar 

  56. Kaeding, W. W., A. T. Shulgin, and E. E. Kenaga: Alkyl-and Amino-Substituted Phenyl N-Methylcarbamate Insecticides. J. agric. Food Chem. 13, 215 (1965).

    Article  CAS  Google Scholar 

  57. Ridgway, R. L.: Systemics for Cotton. Farm Chemicals 128 (6), 82 (1965).

    Google Scholar 

  58. Payne, L. K., H. A. Stansbury, and M. H. J. Weiden: A New Type of Methylcarbamate with Acaricidal Activity. J. med. Chem. 8, 525 (1965).

    Article  CAS  Google Scholar 

  59. Weiden, M. H. J., H. H. Moorefield, and L. K. Payne: O-(methyl-carbamoyl)-oximes: A New Class of Carbamate Insecticide-Acaricides. J. econ. Entomol. 58, 154 (1956).

    Google Scholar 

  60. Payne, L. K., H. A. Stansbury, and M. H. J. Weiden: The Synthesis and Insecticidal Properties of Some Cholinergic Trisubstituted Acetaldehyde O-(Methylcarbamoyl)-Oximes. J. Agric. Food Chem. 14, 356 (1966).

    Article  CAS  Google Scholar 

  61. Addor, R. W.: Synthesis of Dithiolane Oxime Carbamate Insecticides. J. agric. Food Chem. 13, 207 (1965).

    Article  CAS  Google Scholar 

  62. Moorefield, H.: Synergism of the Carbamate Insecticides. Contr. Boyce Thompson Inst. 19, 501 (1958).

    CAS  Google Scholar 

  63. Wilkinson, C. F.: Synergism and the Carbamate Insecticides. Farm Chemicals 129 (10), 48 (1966).

    CAS  Google Scholar 

  64. Adolphi, H.: Examination of a Pyrethrum Synergist. Pyrethrum Post 4 (4), 3 (1958).

    CAS  Google Scholar 

  65. -H. Stummeyer, F. Becke u. H. Sperber: BASF AG, DBP 1029 189, 24.11.55, 30.4.58.

    Google Scholar 

  66. Georghiou, G. P., and R. L. Metcalf: Synergism of Carbamate Insecticides with Octachlordipropyl Ether. J. econ. Entomol. 54, 150 (1961).

    CAS  Google Scholar 

  67. Adams, P., and F. A. Baron: Esters of Carbamic Acid. Chem. Reviews 65, 567 (1965).

    Article  CAS  Google Scholar 

  68. Matzner, M., R. P. Kurkjy, and R. J. Cotter: The Chemistry of Chloroformates. Chem. Reviews 64, 645 (1964).

    Article  CAS  Google Scholar 

  69. Houben-Weyl: Methoden der Organischen Chemie. Sauerstoffverbindungen III, 8, 101 (1952).

    Google Scholar 

  70. -: Methoden der Organischen Chemie. Sauerstoff verbindungen III, 8, 106 (1952).

    Google Scholar 

  71. HeiΒ, R., E. Böcker u. H. Morschel: Farbenfabriken Bayer AG, DBP 1165577, 28.5.60, 19.3.64.

    Google Scholar 

  72. Houben-Weyl: Methoden der Organischen Chemie. Sauerstoffverbindungen III, 8, 119 (1952).

    Google Scholar 

  73. -: Methoden der Organischen Chemie. Sauerstoffverbindungen III, 8, 117 (1952).

    Google Scholar 

  74. Baker, J. W., and J. B. Holdsworth: Kinetic Examination of the Reaction of Aryl Isocyanates with Methyl Alcohol. J. chem. Soc. (London) 713 (1947).

    Google Scholar 

  75. Hopkins, T. R., J. County, and D. D. Strickler: Spencer Chemical Comp., U.S. Patent 3155 713, 5.9.61, 3.11.64.

    Google Scholar 

  76. Tilles, H., and J. Antognini: Stauffer Chemical Comp., U.S. Patent 2913327, 17.1.56, 17.11.59; DBP 1031571, 17.1.57, 4.12.58 (U.S. Priorität 17.1.56).

    Google Scholar 

  77. --Stauffer Chemical Comp., U.S. Patent 3175897, 11.1.57, 30.3.65.

    Google Scholar 

  78. D'Amico, J. J., u. M. W. Harman: Monsanto Chemical Comp., DBP 1142464, 8.5.59, 17.1.63 (U.S. Priorität 28.2.57).

    Google Scholar 

  79. Houben-Weyl: Methoden der Organischen Chemie. Schwefel-, Selen-, Tellur-Verbindungen 9, 808 (1955).

    Google Scholar 

  80. -: Methoden der Organischen Chemie. Schwefel-, Selen-, Tellur-Verbindungen 9, 823 (1955).

    Google Scholar 

  81. Monsanto Chemical Comp., Brit. Patent 882111, 28.2.58, 15.11.61, (U.S. Priorität 28.2.57) und Brit. Patent 956460, 13.7.60, 29.4.64 (U.S. Priorität 13.7.59).

    Google Scholar 

  82. Harman, M. W., and J. J. D'Amico: Monsanto Chemical Comp., U.S. Patent 2744898, 17.3.52, 8.5.56; DBP 1039303, 16.12.54, 18.9.58.

    Google Scholar 

  83. Houben-Weyl: Methoden der Organischen Chemie. Schwefel-, Selen-, Tellur-Verbindungen 9, 837 (1955).

    Google Scholar 

  84. Tisdale, W. H., and I. Williams: E. I. du Pont de Nemours & Comp., U.S. Patent 1972961, 26.5.31, 11.9.34.

    Google Scholar 

  85. Hester, W. F.: Röhm & Haas Comp., U.S. Patent 2 317 765, 20.8.41, 27.4.43.

    Google Scholar 

  86. Dormann, S. C., and A. B. Lindquist: Stauffer Chemical Comp., U.S. Patent 2766554, 28.7.54, 16.10.56. DBP 1013 302.27.6.55,26.8.65.

    Google Scholar 

  87. Flenner, A. L.: E. I. du Pont de Nemours & Comp., U.S. Patent 25 04 404, 12.6.46, 18.4.50.

    Google Scholar 

  88. Thorn, G. D., and R. A. Ludwig: The Dithiocarbamates and Related Compounds. Elsevier Publishing Comp. (Amsterdam — New York), 262 (1962).

    Google Scholar 

  89. Mugno, M.: Montecatini, DBP 1175936, 13.6.60, 13.8.64.

    Google Scholar 

  90. Klöpping, H. L., and G. J. M. van der Kerk: Investigations on Organic Fungicides. IV) Chemical Constitution and Fungistatic Activity of Dithiocarbamates, Thiuramdisulphides and Structurally Related Compounds. Recueil Trav. chim. Pays-Bas 70, 917 (1951).

    Google Scholar 

  91. McCallan, S. E. A.: Agric. Chemicals 1 (7), 15 (1946).

    CAS  Google Scholar 

  92. Martin, L., H. R. Chipman, and C. W. Gates: U.S. Rubber Comp., U.S. Patent 2 859 246, 9.5.55, 4.11.58.

    Google Scholar 

  93. Krzikalla, H., u. O. Flieg: BASF A.G., DBP 928262, 7.12.51, 26.5.55.

    Google Scholar 

  94. Weschky, L., u. O. Flieg: BASF A.G., DBP 919350, 17.1.53, 21.10.54.

    Google Scholar 

  95. Reisener, H., u. H. Schüler: Gebr. Borchers A.G., DBP 1057814, 10.1.56, 21.5.59; DBP 1082 764, 23.8.57, 2.6.60.

    Google Scholar 

  96. Windel, H.: BASF A.G., DBP 1202266, 6.10.61, 12.5.66.

    Google Scholar 

  97. -u. E. H. Pommer: BASF A.G., DBP 1 226 361, 27.3.65, 6.10.66.

    Google Scholar 

  98. Flieg, O., u. H. Windel: BASF A.G., DBP 1 076 434, 17.8.57, 25.2.60; DBP 1 085709, 23.5.59, 21.7.60.

    Google Scholar 

  99. Windel, H., u. E. H. Pommer: BASF A.G., DBP 1 191170, 26.8.61, 16.12.65.

    Google Scholar 

  100. Mugnier, P.: Progil, U.S. Patent 2 855418, 17.1.55, 7.10.58 (Franz. Priorität 17.1.54).

    Google Scholar 

  101. Houben-Weyl: Methoden der Organischen Chemie. Schwefel-, Selen,-Tellur-Verbindungen 9, 853 (1955).

    Google Scholar 

  102. Schlecht, H., L. Weschky u. H. Schroeder: BASF A.G., DBP 1 164391, 31.8.62, 17.9.64.

    Google Scholar 

  103. Houben-Weyl: Methoden der Organischen Chemie. Schwefel-, Selen-, Tellur-Verbindungen 9, 850 (1955).

    Google Scholar 

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Scheuerer, G. (1967). Carbamate als Agrarchemikalien. In: Angewandte Chemie. Fortschritte der Chemischen Forschung, vol 9/2. Springer, Berlin, Heidelberg. https://doi.org/10.1007/BFb0051909

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