Jump to main content
Jump to site search

Issue 1, 2017
Previous Article Next Article

Dehydrative glycosylation with cyclic phosphonium anhydrides

Author affiliations

Abstract

Cyclic phosphonium anhydrides generated from bis-phosphine oxides and trifluoromethanesulfonic anhydride are shown as general coupling reagents in a dehydrative glycosylation reaction of C1-hemiacetals. This reaction protocol is characterized by a broad substrate scope and high yields, including reactions of O-, C-, N-, and S-based nucleophiles with furanose, pyranose, and deoxysugar donors.

Graphical abstract: Dehydrative glycosylation with cyclic phosphonium anhydrides

Back to tab navigation

Supplementary files

Article information


Submitted
18 Aug 2016
Accepted
05 Sep 2016
First published
05 Sep 2016

Org. Biomol. Chem., 2017,15, 51-55
Article type
Communication

Dehydrative glycosylation with cyclic phosphonium anhydrides

R. Dyapa, L. T. Dockery and M. A. Walczak, Org. Biomol. Chem., 2017, 15, 51
DOI: 10.1039/C6OB01812B

Social activity

Search articles by author

Spotlight

Advertisements