STEREOSELECTIVE ALDOL REACTIONS OF GAMMA-THIOBUTYROLACTONE - THE BENZALDEHYDE ANOMALY

被引：4
|
作者：
GENNARI, C
OLIVA, A
MOLINARI, F
PIARULLI, U
机构：
[1] Dipartimento di Chimica Organica e Industriale, Università di Milano, Centro CNR Sost. Org. Nat., 20133 Milano
来源：
TETRAHEDRON LETTERS | 1990年 / 31卷 / 17期
关键词：
D O I：
10.1016/S0040-4039(00)97387-8
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Different protocols (lithium enolate reactions, fluoride catalyzed and Lewis acid mediated silyl ketene acetal reactions) were studied to achieve stereoselectivity in the aldol reactions of γ-thiobutyrolactone: in all cases benzaldehyde showed a striking peculiarity compared to aliphatic aldehydes. © 1990.
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收藏
页码：2453 / 2456
页数：4
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