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HERO ID
8722115
Reference Type
Journal Article
Title
Diastereo- and enantioselective organocatalytic direct conjugate addition of γ-Butenolide to chalcones
Author(s)
Zhang, Y; Yu, C; Ji, Y; Wang, W
Year
2010
Is Peer Reviewed?
Yes
Journal
Chemistry - An Asian Journal
ISSN:
1861-4728
EISSN:
1861-471X
Volume
5
Issue
6
Page Numbers
1303-1306
Language
English
PMID
20397189
DOI
10.1002/asia.201000014
Abstract
A diastereo- and enantioselective conjugate addition reaction of γ-butenolide with chalcones has been developed. Notably, unmodified γ-butenolide was directly employed as a nucleophile in the Michael addition reactions. This process was catalyzed by a previously reported cyclohexane diamine thiourea under mild reaction conditions to afford enantioenriched synthetically and biologically important substituted furanones. 2010 Wiley-VCH Verlag GmbH&Co. KGaA, Weinheim.
Keywords
Enones; Lactones; Michael addition organocatalysis; Thioureas
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