Аннотация:
The 20,20-dimethylacetal group proposed for protection of the 20-oxo group in 21-hydroxylation of steroids by hypervalent iodine compounds has been successfully used to hamper side reactions in microbial 9α- and 11β-hydroxylation and 4-dehydrogenation of 21-hydroxy-16α,17α-epoxypregnanes by Rhodococcus sp., Curvularia lunata and Corynebacterium mediolanum cultures.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
A. M. Turuta, A. V. Kamernitskii, N. E. Voishvillo, N. V. Jlantiashvili, A. P. Krymov, N. V. Domrachev, “Use of 20,20-Dimethylacetal Protection in Microbial Hydroxylation and Dehydrogenation of Steroids”, Mendeleev Commun., 1:3 (1991), 113–114
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5530
https://www.mathnet.ru/rus/mendc/v1/i3/p113
Эта публикация цитируется в следующих 5 статьяx:
Takayuki Yamada, Kodai Saito, Takahiko Akiyama, “Transformation of Trifluorotoluenes Triggered by Titanium(IV) Chloride‐Catalyzed Hydrodefluorination using Hydrosilanes”, Adv Synth Catal, 358:1 (2016), 62
N. E. Voishvillo, A. M. Turuta, A. V. Kamernitsky, “Microorganisms as reagents for transformations of 5?-steroids”, Russ Chem Bull, 43:4 (1994), 515
A. M. Turuta, N. V. Dzhlantiashvili, N. E. Voishvillo, “Transformed steroids”, Russ Chem Bull, 42:5 (1993), 946
A. M. Turuta, T. M. Fadeeva, A. V. Kamernitskii, “Transformed steroids 188. Synthesis routes for 11Β-hydroxy-substituted 16-dehydro-, 17Β-hydroxy- and 16α, 17α,-epoxypregnanes based on 17α-ethynyl-11Β-dihydroxyandrostanes”, Pharm Chem J, 26:3 (1992), 285
A. M. Turuta, A. V. Kamernitskii, T. M. Fadeeva, L. D. Huy, “Transformation of Androsta-4,9-diene-3,17-dione into 16α,17α-Epoxycorticosterone”, Mendeleev Commun., 2:2 (1992), 47–48
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