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Issue 41, 2014
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Novel stereocontrolled amidoglycosylation of alcohols with acetylated glycals and sulfamate ester

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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

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Publication details

The article was received on 18 Mar 2014, accepted on 23 Apr 2014 and first published on 25 Apr 2014


Article type: Communication
DOI: 10.1039/C4RA02367F
Author version available: Download Author version (PDF)
Citation: RSC Adv., 2014,4, 21584-21587
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    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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