Protecting Groups in Carbohydrate Chemistry: Influence on Stereoselectivity of Glycosylations

被引:151
作者
Guo, Jian [1 ]
Ye, Xin-Shan [1 ]
机构
[1] Peking Univ, State Key Lab Nat & Biomimet Drugs, Sch Pharmaceut Sci, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
protecting group; stereoselectivity; glycosylation; carbohydrate; NEIGHBORING-GROUP PARTICIPATION; ALPHA-SELECTIVE GLYCOSYLATIONS; PRE-ACTIVATION PROTOCOL; N-PENTENYL GLYCOSIDES; OLIGOSACCHARIDE SYNTHESIS; ONE-POT; BETA-MANNOPYRANOSYLATION; STEREOCONTROLLED SYNTHESIS; PREACTIVATION PROTOCOL; RADICAL FRAGMENTATION;
D O I
10.3390/molecules15107235
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Saccharides are polyhydroxy compounds, and their synthesis requires complex protecting group manipulations. Protecting groups are usually used to temporarily mask a functional group which may interfere with a certain reaction, but protecting groups in carbohydrate chemistry do more than protecting groups usually do. Particularly, protecting groups can participate in reactions directly or indirectly, thus affecting the stereochemical outcomes, which is important for synthesis of oligosaccharides. Herein we present an overview of recent advances in protecting groups influencing stereoselectivity in glycosylation reactions, including participating protecting groups, and conformation-constraining protecting groups in general.
引用
收藏
页码:7235 / 7265
页数:31
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