Literature DB >> 16209502

A facile method for beta-selenoglycoside synthesis using beta-p-methylbenzoyl selenoglycoside as the selenating unit.

Yumiko Kawai1, Hiromune Ando, Hideya Ozeki, Mamoru Koketsu, Hideharu Ishihara.   

Abstract

[reaction: see text] The reaction between alpha-glycosyl bromides and potassium p-methylselenobenzoate yields beta-p-methylbenzoyl selenoglycosides. The acyl selenoglycosides were activated by the action of a secondary amine and Cs2CO3 to produce an anomeric selenolate anion, which reacted in situ with various electrophiles to yield novel selenoglycosides while retaining the anomeric stereochemistry.

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Year:  2005        PMID: 16209502     DOI: 10.1021/ol051804s

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Convergent synthesis of the pentasaccharide repeating unit of the O-antigenic polysaccharide of enterohaemorrhagic Escherichia coli O113.

Authors:  Abhishek Santra; Anup Kumar Misra
Journal:  Glycoconj J       Date:  2012-05-05       Impact factor: 2.916

2.  Diglycosyl diselenides alter redox homeostasis and glucose consumption of infective African trypanosomes.

Authors:  Jaime Franco; Florencia Sardi; László Szilágyi; Katalin E Kövér; Krisztina Fehér; Marcelo A Comini
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2017-08-12       Impact factor: 4.077

3.  On-water synthesis of glycosyl selenocyanate derivatives and their application in the metal free organocatalytic preparation of nonglycosidic selenium linked pseudodisaccharide derivatives.

Authors:  Tapasi Manna; Anup Kumar Misra
Journal:  RSC Adv       Date:  2021-03-15       Impact factor: 3.361

  3 in total

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