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Recent Developments in the Construction of cis-Glycosidic Linkages

Modem Synthetic Methods in Carbohydrate Chemistry From Monosaccharides to Complex Glycoconjugates, [Pg.97]

First Edition. Edited by Daniel B. Werz and Sebastien Vidal. [Pg.97]

In donor 29, the possible remote anchimeric assistance of the 6-O-acetyl group (vide infra) can also be of beneficial influence to the stereochemical outcome of the glycosylation at hand. To continue the synthesis of the guluronic add tetramer, the 1,6-anhydro-bridge in disaccharide 31 was opened, followed by selective anomeric [Pg.102]

A conceptually different approach to stereoselectively access 1,2-cix-glucosyl and 1,2-cis-galactosyl linkages was recently introduced by Boons and coworkers [31, 32]. [Pg.109]

Besides stereospecific reactions on anomeric triflate intermediates, furanosyl oxocarbenium ions have also been exploited for the introduction of cis-furanosidic [Pg.117]


See other pages where Recent Developments in the Construction of cis-Glycosidic Linkages is mentioned: [Pg.98]    [Pg.114]   


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