ALLYLSILANES IN ORGANIC-SYNTHESIS - STEREOSELECTIVE SYNTHESIS OF TRANS-ALKENE PEPTIDE ISOSTERES

被引：35

作者：

DALY, MJ ^{[1
]}

WARD, RA ^{[1
]}

THOMPSON, DF ^{[1
]}

PROCTER, G ^{[1
]}

机构：

[1] UNIV SALFORD,DEPT CHEM & APPL CHEM,SALFORD M5 4WT,LANCS,ENGLAND

来源：

TETRAHEDRON LETTERS | 1995年 / 36卷 / 41期

关键词：

D O I：

10.1016/0040-4039(95)01528-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Lactones obtained by the diastereoselective dihydroxylation of ester-allylsilanes have been used in the stereocontrolled synthesis of trans-alkene dipeptide isosteres.

引用

页码：7545 / 7548

页数：4

共 20 条

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[6] THE STEREOCHEMISTRY OF THE REACTION OF ALLYLSILANES WITH OSMIUM-TETROXIDE AND OF THE EPOXIDATION AND METHYLENATION OF ALLYLSILANES
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[7] S(N)2' RING-OPENING OF AZIRIDINES BEARING AN ALPHA,BETA-UNSATURATED ESTER GROUP WITH ORGANOCOPPER REAGENTS - A NEW STEREOSELECTIVE SYNTHETIC ROUTE TO (E)-ALKENE DIPEPTIDE ISOSTERES
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[10] ALLYLSILANES IN ORGANIC-SYNTHESIS - AN APPROACH TO THE STEREOSELECTIVE SYNTHESIS OF UNITS FOR NATURAL PRODUCT SYNTHESIS
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