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Experientia

, Volume 24, Issue 2, pp 133–134 | Cite as

Microbiological transformation of 6,14-endo-ethenotetrahydrothebaine alkaloids

  • L. A. Mitscher
  • W. W. Andres
  • G. O. Morton
  • E. L. Patterson
Specialia Chimica. Biochimica. Biophysica

Keywords

Alkaloid Microbiological Transformation 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Zusammenfassung

In der vorliegenden Arbeit werden mikrobiologische Umwandlungen von mehreren 6, 14-endo-Äthenotetrahydrothebain Alkaloiden beschrieben. Mit Hilfe von verschiedenen Mikroorganismen konnten stereospezifische Reduktionen undN-Desalkylierungen ausgeführt werden.

Literatur

  1. 1.
    K. W. Bentley andD. G. Hardy, Proc. chem. Soc.220 (1963).Google Scholar
  2. 2.
    K. W. Bentley andD. G. Hardy, J. Am. chem. Soc.89, 3267 (1967).Google Scholar
  3. 3.
    K. W. Bentley, D. G. Hardy andB. Meek, J. Am. chem. Soc.89, 3273 (1967).PubMedGoogle Scholar
  4. 4.
    K. W. Bentley andD. G. Hardy, J. Am. chem. Soc.89, 3281 (1967).PubMedGoogle Scholar
  5. 5.
    K. W. Bentley, D. G. Hardy andB. Meek, J. Am. chem. Soc.89, 3293 (1967).PubMedGoogle Scholar
  6. 6.
    K. W. Bentley, D. G. Hardy, C. F. Howell, W. Fulmor, J. E. Lancaster, J. J. Brown, G. O. Morton andR. A. Hardy Jr., J. Am. chem. Soc.89, 3303 (1967).PubMedGoogle Scholar
  7. 7.
    K. W. Bentley, D. G. Hardy, H. P. Crocker, D. I. Haddlesey andP. A. Mayor, J. Am. chem. Soc.89, 3312 (1967).PubMedGoogle Scholar
  8. 8.
    W. Fulmor, J. E. Lancaster, G. O. Morton, J. J. Brown, C. F. Howell, C. T. Nora andR. A. Hardy Jr., J. Am. chem. Soc.89, 3322 (1967).PubMedGoogle Scholar
  9. 9.
    A. H. Beckett, Fortschr. ArzneimittForsch.1, 455 (1959).Google Scholar
  10. 10.
    D. H. R. Growley, Fortschr. ArzneimittForsch.7, 11 (1964).Google Scholar
  11. 11.
    K. Aida, K. Uchida, K. Iizuka, S. Okuda, K. Isuda andT. Uemer, Biochem. biophys. Res. Commun.22, 13 (1966).PubMedGoogle Scholar
  12. 12.
    K. Iizuka, M. Yamada, J. Suzuki, I. Seki, K. Aida, S. Okuda, T. Asai andK. Tsuda, Chem. pharm. Bull., Tokyo10, 67 (1962).PubMedGoogle Scholar
  13. 13.
    M. Yamada, K. Iizuka, S. Okuda, T. Asai andK. Tsuda, Chem. pharm. Bull., Tokyo10, 981 (1962).PubMedGoogle Scholar
  14. 14.
    M. Yamada, K. Iizuka, S. Okuda, T. Asai andK. Tsuda, Chem. pharm. Bull., Tokyo11, 206 (1963).Google Scholar
  15. 15.
    M. Yamada, Chem. pharm. Bull., Tokyo11, 356 (1963).Google Scholar
  16. 16.
    G. Schneck, K. H. Froemming andH. G. Schneller, Archs int. Pharmacodyn. Thér.298, 855 (1965).Google Scholar

Copyright information

© Birkhäuser Verlag 1968

Authors and Affiliations

  • L. A. Mitscher
    • 1
  • W. W. Andres
    • 1
  • G. O. Morton
    • 1
  • E. L. Patterson
    • 1
  1. 1.Lederle LaboratoriesA Division of American Cyanamid CompanyPearl RiverUSA

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