Enantioselective synthesis of allylic alcohols by the sequential aminoxylation-olefination reactions of aldehydes under ambient conditions

被引：89
作者：
Zhong, GF
Yu, YP
机构：
[1] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[3] Torrey Pines Inst Mol Studies, San Diego, CA 92121 USA
来源：
ORGANIC LETTERS | 2004年 / 6卷 / 10期
关键词：
D O I：
10.1021/ol049524k
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A novel, highly enantioselective synthesis of O-amino-substituted allylic alcohols by the sequential asymmetric alpha-aminoxylation/Wadsworth-Emmons-Horner olefination reactions of aldehydes is presented.
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页码：1637 / 1639
页数：3
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