Literature DB >> 12240014

Epoxidation of allylic alcohols in aqueous solutions of non surfactant amphiphilic sugars.

C Denis1, K Misbahi, A Kerbal, V Ferrières, D Plusquellec.   

Abstract

A variety of cyclic and acyclic allylic alcohols undergo efficient chemo-, regio- and/or stereoselective epoxidations in neutral aqueous solutions of amphiphilic carbohydrates (sucrose, L-arabinose, methyl or ethyl beta-D-fructopyranoside) by using dilute hydrogen peroxide in the presence of molybdic or tungstic salts.

Entities:  

Year:  2001        PMID: 12240014     DOI: 10.1039/b108352j

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  Tungsten-catalyzed asymmetric epoxidation of allylic and homoallylic alcohols with hydrogen peroxide.

Authors:  Chuan Wang; Hisashi Yamamoto
Journal:  J Am Chem Soc       Date:  2014-01-21       Impact factor: 15.419

  1 in total

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