Issue 41, 2014

Novel stereocontrolled amidoglycosylation of alcohols with acetylated glycals and sulfamate ester

Abstract

A regio- and stereo-controlled, one-pot amidoglycosylation of alcohols has been achieved using O-acetylated glycals, trichloroethoxysulfonamide, and iodosobenzene in the presence of a rhodium(II) catalyst. The reaction would proceed via stereoselective intermolecular aziridination of the glycal.

Graphical abstract: Novel stereocontrolled amidoglycosylation of alcohols with acetylated glycals and sulfamate ester

Supplementary files

Article information

Article type
Communication
Submitted
18 Mar 2014
Accepted
23 Apr 2014
First published
25 Apr 2014

RSC Adv., 2014,4, 21584-21587

Author version available

Novel stereocontrolled amidoglycosylation of alcohols with acetylated glycals and sulfamate ester

T. Murakami, Y. Sato, K. Yoshioka and M. Tanaka, RSC Adv., 2014, 4, 21584 DOI: 10.1039/C4RA02367F

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