Glycosylation Employing Unprotected Carbohydrate Acceptor Components

Author(s): Stephan Bottcher, Joachim Thiem.

Journal Name: Current Organic Chemistry

Volume 18 , Issue 14 , 2014

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Abstract:

This review discusses concepts towards facile non-enzymatic glycosylation of unprotected or lightly protected glycostructures. These comprise approaches in which reactivity distinction of hydroxyl groups is achieved via stannylene or boronic and borinic acid intermediates as well as via oxyanion formation along with syntheses based on selectivity implemented by the substrates themselves. Further, syntheses of complex glycostructures and oligosaccharides are shown, as well as the concept of random glycosylation towards glycoside libraries with desired equal product distribution.

Keywords: Base promoted, boronic/borinic acid mediated, glycosylation, random approach, stannylene-mediated, substance controlled, unprotected/partially protected acceptors.

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Article Details

VOLUME: 18
ISSUE: 14
Year: 2014
Page: [1804 - 1817]
Pages: 14
DOI: 10.2174/1385272819666140527231701
Price: $58

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