Extending the possibility of an N-Troc-protected sialic acid donor toward variant sialo-glycoside synthesis

被引:115
作者
Ando, H
Koike, Y
Ishida, H
Kiso, M
机构
[1] Gifu Univ, Dept Appl Bioorgan Chem, Gifu 5011193, Japan
[2] Japan Sci & Technol Corp, CREST, Gifu 5011193, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
N-Troc group; sialidation; sialic acid analogs;
D O I
10.1016/S0040-4039(03)01707-6
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The potential of an N-Troc-protected sialic acid donor, equipped with phenylsulfenyl functionality as a leaving group, has been explored. As a result, the entitled donor was proven to be highly reactive and to have broad applicability toward the synthesis of variant sialo-glycans, which have N-glycolyl, de-N-acetyl, 1,5-lactam and 8-O-sulfo sialic acid analogs. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6883 / 6886
页数:4
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