STEREOSELECTIVE SYNTHESIS OF THE AONIDIELLA-CITRINA SEX PHEROMONE (3S,5E)-(-)-3,9-DIMETHYL-6-ISOPROPYLDECA-5,8-DIEN-1-YL ACETATE

被引：8

作者：

BAUDOUY, R ^{[1
]}

SANCHO, MR ^{[1
]}

机构：

[1] UNIV LYON 1,CNRS,URA 467,CHIM ORGAN LAB 1,F-69622 VILLEURBANNE,FRANCE

来源：

TETRAHEDRON | 1991年 / 47卷 / 48期

关键词：

D O I：

10.1016/S0040-4020(01)96050-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The stereospecific elaboration of the trisubstituted double bond of acetate 1, is realized by condensation of an alpha-silylaldimine with aldehyde A prepared from (-)-citronellol.

引用

页码：10015 / 10022

页数：8

共 24 条

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[8] A HIGHLY SELECTIVE METHOD FOR THE SYNTHESIS OF (E)-ALPHA-METHYL-ALPHA,BETA-UNSATURATED ALDEHYDES
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[9] ASYMMETRIC MICHAEL ADDITIONS VIA SAMP-RAMP-HYDRAZONES ENANTIOSELECTIVE SYNTHESIS OF BETA-SUBSTITUTED DELTA-OXOPENTANOATES AND DELTA-LACTONES
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