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Microbiological transformation of 6,14-endo-ethenotetrahydrothebaine alkaloids.

作者信息

Mitscher L A, Andres W W, Morton G O, Patterson E L

出版信息

Experientia. 1968 Feb 15;24(2):133-4. doi: 10.1007/BF02146941.

DOI:10.1007/BF02146941
PMID:5643799
Abstract
摘要

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N-demethylation of nicotine and reduction of nicotine-1'-N-oxide by Microsporum gypseum.石膏样小孢子菌对尼古丁的N-去甲基化作用及对尼古丁-1'-N-氧化物的还原作用。
Appl Environ Microbiol. 1979 Nov;38(5):836-9. doi: 10.1128/aem.38.5.836-839.1979.

本文引用的文献

1
[Studies in the field of microbiological decomposition. XVII. Transformation of alkaloids in the morphine series by Trametes sanguinea. (2)].[微生物分解领域的研究。十七。血红栓菌对吗啡系列生物碱的转化。(2)]
Chem Pharm Bull (Tokyo). 1962 Oct;10:981-4.
2
[Studies in the field of microbiological decomposition. XVI. Decomposition of alkaloids of the morphine group by Trametes sanguinea].[微生物分解领域的研究。十六。血红栓菌对吗啡类生物碱的分解]
Chem Pharm Bull (Tokyo). 1962 Jan;10:67-70. doi: 10.1248/cpb.10.67.
3
Stereochemical factors in biological activity.
Fortschr Arzneimittelforsch. 1959;1:455-530. doi: 10.1007/978-3-0348-7035-1_6.
4
Nuclear magnetic resonance studies in the 6,14-endo-ethenotetrahydrothebaine series.6,14-内-乙烯基四氢蒂巴因系列的核磁共振研究。
J Am Chem Soc. 1967 Jun 21;89(13):3322-30. doi: 10.1021/ja00989a601.
5
Novel analgesics and molecular rearrangements in the morphine-thebaine group. VI. Base-catalyzed rearrangements in the 6,14-endo-ethenotetrahydrothebaine series.
J Am Chem Soc. 1967 Jun 21;89(13):3312-21. doi: 10.1021/ja00989a035.
6
Novel analgesics and molecular rearrangements in the morphine-thebaine group. V. Derivatives of 7,8-dihydrocyclohexeno[1',2':8,14]codeinone.
J Am Chem Soc. 1967 Jun 21;89(13):3303-11. doi: 10.1021/ja00989a034.
7
Novel analgesics and molecular rearrangements in the morphine-thebaine group. IV. Acid-catalyzed rearrangements of alcohols of the 6,14-endo-ethenotetrahydrothebaine series.吗啡-蒂巴因类中的新型镇痛药及分子重排。IV. 6,14-内-乙烯基四氢蒂巴因系列醇的酸催化重排
J Am Chem Soc. 1967 Jun 21;89(13):3293-303. doi: 10.1021/ja00989a033.
8
Novel analgesics and molecular rearrangements in the morphine-thebaine group. 3. Alcohols of the 6,14-endo-ethenotetrahydrooripavine series and derived analogs of N-allylnormorphine and -norcodeine.
J Am Chem Soc. 1967 Jun 21;89(13):3281-92. doi: 10.1021/ja00989a032.
9
Novel analgesics and molecular rearrangements in the morphine-thebaine group. II. Alcohols derived from 6,14-endo-etheno- and 6,14-endo-ethanotetrahydrothebaine.
J Am Chem Soc. 1967 Jun 21;89(13):3273-80. doi: 10.1021/ja00989a031.
10
Incorporation of molecular oxygen into a morphine alkaloid, 14-hydroxycodeinone by Trametes sanguinea.血红栓菌将分子氧掺入吗啡生物碱14-羟基可待因酮中。
Biochem Biophys Res Commun. 1966 Jan 4;22(1):13-6. doi: 10.1016/0006-291x(66)90594-8.