AN EXPEDITIOUS ENANTIOSPECIFIC SYNTHESIS OF A PRECURSOR OF THE LACTONIC PORTION OF MEVINIC ACIDS

被引：12

作者：

BOQUEL, P ^{[1
]}

CAZALET, CL ^{[1
]}

CHAPLEUR, Y ^{[1
]}

SAMRETH, S ^{[1
]}

BELLAMY, F ^{[1
]}

机构：

[1] LAB FOURNIER,RES CTR,F-21121 DAIX,FRANCE

来源：

TETRAHEDRON LETTERS | 1992年 / 33卷 / 15期

关键词：

HMGCOA REDUCTASE; LEVOGLUCOSAN; THIONOCARBONATE; RADICAL DEOXYGENATION;

D O I：

10.1016/0040-4039(92)88123-M

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A short, enantiospecific synthesis of the methylglycoside 5, a precursor of the lactonic moiety present in all mevinic acids and analogues, starting with 1,6-anhydro-D-glucose is described.

引用

页码：1997 / 2000

页数：4

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