Literature DB >> 11125832

A mild and selective cleavage of trityl ethers by CBr4-MeOH.

J S Yadav1, B V Subba Reddy.   

Abstract

Trityl ethers are selectively deprotected to the corresponding alcohols in high yields by CBr4 in refluxing methanol under neutral reaction conditions. Other hydroxyl protecting groups like isopropylidene, allyl, benzyl, acetyl, benzoyl, methyl, tosyl, prenyl, propargyl, tert-butyldiphenylsilyl and p-methoxybenzyl ethers are unaffected.

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Year:  2000        PMID: 11125832     DOI: 10.1016/s0008-6215(00)00241-x

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  1 in total

1.  Inhibition of S-ribosylhomocysteinase (LuxS) by substrate analogues modified at the ribosyl C-3 position.

Authors:  Stanislaw F Wnuk; Jenay Robert; Adam J Sobczak; Brandon P Meyers; Venkata L A Malladi; Jinge Zhu; Bhaskar Gopishetty; Dehua Pei
Journal:  Bioorg Med Chem       Date:  2009-07-26       Impact factor: 3.641

  1 in total

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