Synthesis of five-membered homothiosugars derived from L-erythrose and D-mannose

被引：8

作者：

Riedner, J ^{[1
]}

Robina, I ^{[1
]}

Fernández-Bolaños, JG ^{[1
]}

Gómez-Bujedo, S ^{[1
]}

Fuentes, J ^{[1
]}

机构：

[1] Univ Seville, Fac Quim, Dept Quim Organ, E-41071 Seville, Spain

来源：

TETRAHEDRON-ASYMMETRY | 1999年 / 10卷 / 17期

关键词：

D O I：

10.1016/S0957-4166(99)00365-1

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The synthesis of homothiosugars by conjugate addition of the hydrogen sulfide anion to the double bond of alpha,beta-unsaturated esters followed by nucleophilic internal displacement of a sulfonyloxy group is described. The new thiolanes were evaluated as enzyme inhibitors. (C) 1999 Elsevier Science Ltd. All rights reserved.

引用

页码：3391 / 3401

页数：11

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