Free radical brominative ring opening of 1,2-O-benzylidene pyranoses: a route to glycosylating agents

Publisher Website
Google Scholar
Abstract
Bromination of fully protected 1,2-O-benzylidenated pyranoses with bromotrichloromethane and u.v. light or N-bromosuccinimide gives 2-O-benzoyl glycosyl bromides in good yields, which may be converted in situ to glycosides and disaccharides.

This publication has 0 references indexed in Scilit: