前往化源商城

Organic letters

Protecting group free glycosidations using p-toluenesulfonohydrazide donors

AV Gudmundsdottir, M Nitz

文献索引:Gudmundsdottir, Anna V.; Nitz, Mark Organic Letters, 2008 , vol. 10, # 16 p. 3461 - 3463

全文:HTML全文

被引用次数: 40

摘要

N′-Glycopyranosylsulfonohydrazides are introduced as glycosyl donors for protecting group free synthesis of O-glycosides, glycosyl azides, and oxazolines. Mono-and disaccharides containing a reducing terminal N-acetylglucosamine residue were condensed with p-toluenesulfonylhydrazide to give the desired β-d-pyranose donors. These donors can be activated with NBS and then glycosidated with the desired alcohol or transformed to ...