REGIOSELECTIVE SULFATION OF GALACTOSE DERIVATIVES THROUGH THE STANNYLENE PROCEDURE - NEW SYNTHESIS OF THE 3'-O-SULFATED LEWIS(A) TRISACCHARIDE

被引：51

作者：

LUBINEAU, A

LEMOINE, R

机构：

[1] Institut de Chimie Moléculaire d'Orsay, Laboratoire de Chimie Organique Multifonctionnelle, associé au CNRS, 91405 Orsay Cedex

来源：

TETRAHEDRON LETTERS | 1994年 / 35卷 / 47期

关键词：

D O I：

10.1016/S0040-4039(00)78500-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Free or 6-protected beta-D-galactopyranosides afforded, in excellent yields, the 3'-O-sulfate as the only product through the stannylene procedure. This methodology was successfully applied to the synthesis of the 3'-O-sulfated Lewis(a) trisaccharide, an oligosaccharide reported as ligand of E- and L-selectins.

引用

页码：8795 / 8796

页数：2

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