Recent Advances in Chemical Synthesis of Amino Sugars

被引:3
|
作者
Yang, Jian [1 ,2 ]
Xie, Demeng [1 ]
Ma, Xiaofeng [1 ,2 ]
机构
[1] Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
来源
MOLECULES | 2023年 / 28卷 / 12期
基金
中国国家自然科学基金;
关键词
amino sugars; biological activities; stereoselective synthesis; glycosylation; INTERMOLECULAR AGLYCON TRANSFER; N-HETEROCYCLIC CARBENE; CATALYZED STEREOSELECTIVE GLYCOSYLATION; CONVERGENT SYNTHESIS; ALPHA-GLYCOSYLATION; PROTECTING GROUP; GLYCOSYLPHOSPHATIDYLINOSITOL ANCHOR; SELECTIVE GLYCOSYLATION; OLIGOSACCHARIDE SYNTHESIS; DIVERSIFIED SYNTHESIS;
D O I
10.3390/molecules28124724
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
Amino sugars are a kind of carbohydrates with one or more hydroxyl groups replaced by an amino group. They play crucial roles in a broad range of biological activities. Over the past few decades, there have been continuing efforts on the stereoselective glycosylation of amino sugars. However, the introduction of glycoside bearing basic nitrogen is challenging using conventional Lewis acid-promoted pathways owing to competitive coordination of the amine to the Lewis acid promoter. Additionally, diastereomeric mixtures of O-glycoside are often produced if aminoglycoside lack a C2 substituent. This review focuses on the updated overview of the way to stereoselective synthesis of 1,2-cis-aminoglycoside. The scope, mechanism, and the applications in the synthesis of complex glycoconjugates for the representative methodologies were also included.
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页数:49
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