Enantioselective synthesis of (+)-α-vetivone through the Michael reaction of chiral imines

被引:28
作者
Revial, G
Jabin, I
Pfau, M
机构
[1] ESPCI, CNRS, ESA 7084, Chim Organ Lab, F-75231 Paris 05, France
[2] Univ Havre, URCOM, Fac Sci & Tech, F-76058 Le Havre, France
关键词
D O I
10.1016/S0957-4166(00)00481-X
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
(+)-alpha -Vetivone has been synthesised in nine steps. The absolute stereochemistry of the two stereogenic centres is controlled in the same key step involving the stereoselective Michael addition of a chiral imine of 4-isopropylidene-2-methylcyclohexanone to phenyl crotonate. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:4975 / 4983
页数:9
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