New protecting groups in the synthesis of oligosaccharides

被引：14

作者：

Polyakova, S. M. ^{[1
]}

Nizovtsev, A. V. ^{[2
]}

Kunetskiy, R. A. ^{[2
]}

Bovin, N. V. ^{[1
]}

机构：

[1] Russian Acad Sci, MM Shemyakin & Yu A Ovchinnikov Inst Bioorgan Che, 16-10 Ul Miklukho Maklaya, Moscow 117997, Russia

[2] LSS Semiot, 16-10 Ul Miklukho Maklaya, Moscow 117997, Russia

来源：

RUSSIAN CHEMICAL BULLETIN | 2015年 / 64卷 / 05期

基金：

俄罗斯科学基金会;

关键词：

protecting groups; oligosaccharides; carbohydrates; glycosylation; INTRAMOLECULAR AGLYCON DELIVERY; NEIGHBORING GROUP PARTICIPATION; STEREOSELECTIVE-SYNTHESIS; ETHER GROUP; BLOCK SYNTHESIS; NAP ETHER; GROUP-A; GLUCOSAMINE; GLYCOSYLATION; VERSATILE;

D O I：

10.1007/s11172-015-0968-5

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The review is focused on new hydroxy and amino protecting groups in carbohydrate chemistry developed or gained popularity over the last 15 years. Representative examples for the protecting group manipulations are given.

引用

页码：973 / 989

页数：17

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[41] New Strategies for the Synthesis of Bio-medically Relevant Oligosaccharides: Recent Updates on 1,2-cis-O-Glycosylation and α-O-Sialylation [J].

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