Literature DB >> 10705498

A facile synthesis of 2-deoxy-2,3-didehydroneuraminic acid derivatives.

K Ikeda1, K Konishi, K Sano, K Tanaka.   

Abstract

The 2-thio- or 2-selenoglycosides of N-acetylneuraminic acid methyl ester were transformed by successive treatment with dimethyl(methylthio)sulfonium triflate (DMTST) and 1,8-diazabicyclo[5.4.0]-7-undecene (DBU) to give the corresponding methyl 2-deoxy-2,3-didehydroneuraminates in excellent yields. Their acids and their analogues are sialidase inhibitors of pharmaceutical interest.

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Year:  2000        PMID: 10705498     DOI: 10.1248/cpb.48.163

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  2 in total

1.  One-pot SSA-catalyzed β-elimination: an efficient and inexpensive protocol for easy access to the glycal of sialic acid.

Authors:  Erickson M Paragas; I Abrrey Monreal; Chris M Vasil; Jonel P Saludes
Journal:  Carbohydr Res       Date:  2014-09-17       Impact factor: 2.104

2.  Efficient method for the preparation of peracetylated Neu5Ac2en by flash vacuum pyrolysis.

Authors:  Evan J Horn; Jacquelyn Gervay-Hague
Journal:  J Org Chem       Date:  2009-06-05       Impact factor: 4.354

  2 in total

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