Literature DB >> 10649376

Acetamidoglycosylation with Glycal Donors: A One-Pot Glycosidic Coupling with Direct Installation of the Natural C(2)-N-Acetylamino Functionality.

V Di Bussolo1, J Liu, L G Huffman, D Y Gin.   

Abstract

Nitrogen transfer to glycals: A new method for direct C2-aza-glycosylation with glycal donors has been developed (see scheme), employing the new reagent combination of thianthrene-S-oxide and trifluoroacetic anhydride for glycal activation, in an overall one-pot procedure.

Entities:  

Year:  2000        PMID： 10649376     DOI： 10.1002/(sici)1521-3773(20000103)39:1<204::aid-anie204>3.3.co;2-q

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


  2 in total

Review 1.  Chemical glycosylation in the synthesis of glycoconjugate antitumour vaccines.

Authors:  Danica P Galonić; David Y Gin
Journal:  Nature       Date:  2007-04-26       Impact factor: 49.962

2.  Protecting group and solvent control of stereo- and chemoselectivity in glucal 3-carbamate amidoglycosylation.

Authors:  Ritu Gupta; Kimberly M Sogi; Sarah E Bernard; John D Decatur; Christian M Rojas
Journal:  Org Lett       Date:  2009-04-02       Impact factor: 6.005
  2 in total

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