Literature DB >> 24199837

Synthesis of a C-glycoside analogue of β-galactosyl ceramide, a potential HIV-1 entry inhibitor.

V Narasimharao Thota1, Mula Brahmaiah, Suvarn S Kulkarni.   

Abstract

A β-C-galactosyl ceramide was synthesized in a stereoselective manner, employing a Sharpless AD reaction and olefin cross metathesis as key steps.

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Year:  2013        PMID： 24199837     DOI： 10.1021/jo402115w

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


  2 in total

1.  An organocatalytic strategy for the stereoselective synthesis of C-galactosides with fluorine at the pseudoanomeric carbon.

Authors:  Ahmad S Altiti; S Bachan; W Alrowhani; D R Mootoo
Journal:  Org Biomol Chem       Date:  2015-11-07       Impact factor: 3.876

2.  C-glycosphingolipid precursors via iodocyclization of homoallyic trichloroacetimidates.

Authors:  Ahmad S Altiti; David R Mootoo
Journal:  Carbohydr Res       Date:  2015-02-21       Impact factor: 2.104
  2 in total

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