An efficient diastereoselective synthesis of β-1-formyl-2,3,4,6-tetra-O-benzyl-D-glucopyranoside

被引：20

作者：

Labéguère, F ^{[1
]}

Lavergne, JP ^{[1
]}

Martinez, J ^{[1
]}

机构：

[1] Univ Montpellier 2, CNRS, UMR 5810, Lab Aminoacides Peptides & Prot, F-34095 Montpellier 5, France

来源：

TETRAHEDRON LETTERS | 2002年 / 43卷 / 40期

关键词：

D O I：

10.1016/S0040-4039(02)01477-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A diastereoselective synthesis of beta-1-formyl-2,3,4,6-tetra-O-benzyl-D-glucopyranoside in four steps, using an umpolung Seebach reaction is described. (C) 2002 Elsevier Science Ltd. All rights reserved.

引用

页码：7271 / 7272

页数：2

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