Literature DB >> 23237834

Alkoxyamino glycoside acceptors for the regioselective synthesis of oligosaccharides using glycosynthases and transglycosidases.

David Teze1, Michel Dion, Franck Daligault, Vinh Tran, Corinne André-Miral, Charles Tellier.   

Abstract

Alkoxyamino derivatives of oligosaccharides have been synthesized by enzymatic synthesis using a glycosynthase and a transglycosidase. The chemoselective assembly of unprotected oligosaccharides bearing glucose at the reducing end with N-alkyl-O-benzylhydroxylamine provides sugar derivatives that are good acceptors for enzymatic synthesis using either glycosynthase or transglycosidase. Furthermore, this method affords the possibility of controlling the regioselectivity of coupling depending on the nature of the alkoxyamino substituent and provides high-yield coupling of sugars without the need for complex protecting group chemistry.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 23237834     DOI: 10.1016/j.bmcl.2012.11.065

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Neoglycosylation and neoglycorandomization: Enabling tools for the discovery of novel glycosylated bioactive probes and early stage leads.

Authors:  Randal D Goff; Jon S Thorson
Journal:  Medchemcomm       Date:  2014-08-01       Impact factor: 3.597

2.  DNA-Templated N(Me)-Alkoxyamine Glycosylation.

Authors:  Tommi Österlund; Heidi Korhonen; Pasi Virta
Journal:  Org Lett       Date:  2018-03-07       Impact factor: 6.005

  2 in total

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