Sulfonomethyl analogues of aldos-2-ulosonic acids.: Synthesis of a new sialyl Lewis X analogue

被引：23

作者：

Borbás, A

Szabovik, G

Antal, Z

Herczegh, P

Agócs, A

Lipták, A

机构：

[1] Hungarian Acad Sci, Antibiot Res Grp, H-4010 Debrecen, Hungary

[2] Hungarian Acad Sci, Res Grp Carbohydrates, H-4010 Debrecen, Hungary

[3] Lajos Kossuth Univ, Inst Biochem, H-4010 Debrecen, Hungary

来源：

TETRAHEDRON LETTERS | 1999年 / 40卷 / 18期

基金：

匈牙利科学研究基金会;

关键词：

carbohydrates; sulfonic acid derivatives; thioglycosides; glycosidation;

D O I：

10.1016/S0040-4039(99)00522-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Sulfonomethyl derivatives of aldos-2-ulosonic acids have been synthesized by addition of the ethyl methanesulfonate carbanion to aldonolactones. A sulfonylated mimic molecule of the sialyl Lewis X tetrasaccharide has been prepared by using a new sulfonomethyl ulosonic acid analogue. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.

引用

收藏

页码：3639 / 3642

页数：4

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