The stereoselective synthesis of a key intermediate of the trinem antibiotic Sanfetrinem

被引：22

作者：

Ghiron, C ^{[1
]}

Piga, E ^{[1
]}

Rossi, T ^{[1
]}

Tamburini, B ^{[1
]}

Thomas, RJ ^{[1
]}

机构：

[1] GLAXO WELLCOME SPA,MED RES CTR,I-37135 VERONA,ITALY

来源：

TETRAHEDRON LETTERS | 1996年 / 37卷 / 22期

关键词：

D O I：

10.1016/0040-4039(96)00682-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

By modulating the reactivity of the Lewis acid promoter it was possible to obtain, in a single stereoselective condensation step, the methoxyketone 7, an advanced intermediate in the synthesis of Sanfetrinem GV104326. Copyright (C) 1996 Elsevier Science Ltd

引用

页码：3891 / 3894

页数：4

共 6 条

[1] THE SYNTHESIS OF A KEY INTERMEDIATE OF TRICYCLIC BETA-LACTAM ANTIBIOTICS [J].