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A diastereoselective phenylselenium-induced lactamization of olefinic amides. A possible route to alpha- and beta-amino acid derivatives SCIE SCOPUS

Title
A diastereoselective phenylselenium-induced lactamization of olefinic amides. A possible route to alpha- and beta-amino acid derivatives
Authors
Chung, SKJeong, THKang, DH
Date Issued
1997-01-09
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Abstract
The organoselenium-induced cyclofunctionalization of (S)-N-(alpha,beta-unsaturated-acyl)prolinamides was found to produce with a high degree of chirality transfer, 7- and 6-membered bislactam derivatives depending on the substitution pattern of the starting material. (C) 1997 Published by Elsevier Science Ltd.
Keywords
STEREOSELECTIVE SYNTHESIS; CYCLIZATION; LACTAMS; OXIMES
URI
https://oasis.postech.ac.kr/handle/2014.oak/21395
DOI
10.1016/S0957-4166(96)00496-X
ISSN
0957-4166
Article Type
Article
Citation
TETRAHEDRON-ASYMMETRY, vol. 8, no. 1, page. 5 - 9, 1997-01-09
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