Transformed steroids. Communication 156. Reaction of pregn-5-ene-3β,17α-diol-20-one and its 16α-methyl derivative with iodosobenzene diacetate; a one-step method for the synthesis of 17-spirooxetan-20-ones Научная публикация
Журнал |
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science
ISSN: 2376-8444 , E-ISSN: 0568-5230 |
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Вых. Данные | Год: 1986, Том: 35, Номер: 8, Страницы: 1720-1723 Страниц : 4 DOI: 10.1007/bf00954623 | ||
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Реферат:
The main path of the reaction of 17α-hydroxypregnenolone and its 16α-methyl analog with iodosobenzene diacetate in a methanol solution of an alkali is intramolecular cyclization with the formation of 17-spiro-oxetan-20-ones.
Библиографическая ссылка:
Turuta A.M.
, Kamernitskii A.V.
, Fadeeva T.M.
, Zhulin A.V.
Transformed steroids. Communication 156. Reaction of pregn-5-ene-3β,17α-diol-20-one and its 16α-methyl derivative with iodosobenzene diacetate; a one-step method for the synthesis of 17-spirooxetan-20-ones
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science. 1986. V.35. N8. P.1720-1723. DOI: 10.1007/bf00954623 OpenAlex
Transformed steroids. Communication 156. Reaction of pregn-5-ene-3β,17α-diol-20-one and its 16α-methyl derivative with iodosobenzene diacetate; a one-step method for the synthesis of 17-spirooxetan-20-ones
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science. 1986. V.35. N8. P.1720-1723. DOI: 10.1007/bf00954623 OpenAlex
Идентификаторы БД:
OpenAlex: | W2313121590 |
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Пока нет цитирований