PHEROMONE SYNTHESIS .84. ENHANCEMENT OF OPTICAL PURITY OF A PRODUCT BY REMOVING UNWANTED DIASTEREOMERS IN THE COURSE OF A CHIRAL SYNTHESIS - NEW SYNTHESIS OF THE STEREOISOMERS OF 2,8-DIMETHYL-1,7-DIOXASPIRO[5.5]UNDECANE, THE PHEROMONE OF ANDRENA WILKELLA

被引：56

作者：

MORI, K

WATANABE, H

机构：

来源：

TETRAHEDRON | 1986年 / 42卷 / 01期

关键词：

D O I：

10.1016/S0040-4020(01)87431-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：295 / 304

页数：10

共 17 条

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[10] SYNTHESIS OF THE ENANTIOMERS OF 3-HYDROXY-1,7-DIOXASPIRO[5.5]UNDECANE, A MINOR COMPONENT OF THE OLIVE FLY PHEROMONE [J].

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