Literature DB >> 26251305

First Total Synthesis of Trehalose-Containing Branched Oligosaccharide OSE-1 of Mycobacterium gordonae (Strain 990).

Manishkumar A Chaube1, Suvarn S Kulkarni2.   

Abstract

The first total synthesis of the branched oligosaccharide OSE-1 of Mycobacterium gordonae (strain 990) is reported. An intramolecular aglycon delivery approach was used for constructing the desymmetrized 1,1'-α,α-linked trehalose moiety. A [3+2] glycosylation of the trisaccharide donor and trehalose acceptor furnished the right hand side pentasaccharide. Regioselective O3 glycosylation of L-rhamnosyl 2,3-diol allowed expedient synthesis of the left hand side tetrasaccharide. The nonasaccharide was assembled in a highly convergent fashion through a [4+5] glycosylation.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Keywords:  1,1′-α,α-glycosylation; Mycobacterium gordonae; regioselective glycosylation; total synthesis; trehalose oligosaccharides

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Year:  2015        PMID: 26251305     DOI: 10.1002/chem.201502521

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  2 in total

1.  Tailoring Trehalose for Biomedical and Biotechnological Applications.

Authors:  Mara K O'Neill; Brent F Piligian; Claire D Olson; Peter J Woodruff; Benjamin M Swarts
Journal:  Pure Appl Chem       Date:  2017-01-11       Impact factor: 2.453

2.  AuCl3-Catalyzed Hemiacetal Activation for the Stereoselective Synthesis of 2-Deoxy Trehalose Derivatives.

Authors:  Robin Jeanneret; Carlo Walz; Maarten van Meerbeek; Sarah Coppock; M Carmen Galan
Journal:  Org Lett       Date:  2022-08-22       Impact factor: 6.072

  2 in total

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