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This article is cited in 1 scientific paper (total in 1 paper)
Synthesis of enantiopure 1,3,4-thiazaphospholes
L. K. Kibardina, M. A. Pudovik, V. A. Alfonsov, O. N. Kataeva
A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
Abstract:
Racemic and (R)-(+)-N-trimethylsilyl-(1-phenyl)ethylamines stereoselectively react with O-phenylchloromethylisothiocyanatothiophosphonate to give a diastereomeric mixture of separable 1,3,4-thiazaphospholes; racemic thiazaphosphole crystallises as a conglomerate.
Keywords:
Thiazaphosphole, Racemic and R-(+)-N-trimethylsilyl-(1-phenyl)ethylamines, Cyclization reaction, diastereoselectivity.
Citation:
L. K. Kibardina, M. A. Pudovik, V. A. Alfonsov, O. N. Kataeva, “Synthesis of enantiopure 1,3,4-thiazaphospholes”, Mendeleev Commun., 17:6 (2007), 323–324
Linking options:
https://www.mathnet.ru/eng/mendc3475 https://www.mathnet.ru/eng/mendc/v17/i6/p323
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