ITERATIVE SYN-1,3,5-TRIOL SYNTHESIS UTILIZING THE REACTION OF BETA-(TRIMETHYLSILYL)ALKYL PHENYL SULFONES WITH OXIRANES

被引：12

作者：

ACHMATOWICZ, B ^{[1
]}

WICHA, J ^{[1
]}

机构：

[1] POLISH ACAD SCI,INST ORGAN CHEM,UL KASPRZAKA 44,PL-01224 WARSAW,POLAND

来源：

TETRAHEDRON-ASYMMETRY | 1993年 / 4卷 / 03期

关键词：

D O I：

10.1016/S0957-4166(00)86085-1

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Partly protected triols 8a and 8b were synthesised from epoxide 1 using beta-trimethylsilyl sulphones 2a and 2a for the chain elongation and the Cardillo procedure for diastereoselective two-step epoxidation of homoallylic alcohols.

引用

页码：399 / 410

页数：12

共 21 条

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[9] THE REACTION OF BETA-(TRIMETHYLSILYL)ALKYL PHENYL SULFONES WITH OXIRANES - A METHOD FOR STEREOCONTROLLED SYNTHESIS OF HOMOALLYLIC ALCOHOLS
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