A versatile scaffold for a library of liposidomycins analogues: A crucial and potent glycosylation step

被引：15

作者：

Gravier-Pelletier, C ^{[1
]}

Ginisty, M ^{[1
]}

Le Merrer, Y ^{[1
]}

机构：

[1] Univ Paris 05, UMR 8601 CNRS, Lab Chim & Biochim Pharmacol & Toxicol, F-75270 Paris 06, France

来源：

TETRAHEDRON-ASYMMETRY | 2004年 / 15卷 / 02期

关键词：

D O I：

10.1016/j.tetasy.2003.10.017

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

A key step for the synthesis of a diazepanone scaffold dedicated to a library of MraY inhibitors is described. It involves the O-glycosylation of a conveniently protected L-serine by a D-ribofuranose derivative. High yield and selectivity were obtained. (C) 2003 Elsevier Ltd. All rights reserved.

引用

页码：189 / 193

页数：5