Published in
Royal Society of Chemistry, Chemical Communications, 23, p. 2460-2461
DOI: 10.1039/b108352j
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Epoxidation of allylic alcohols in aqueous solutions of non surfactant amphiphilic sugars
Journal article published in 2001 by
Cécile Denis,
Khalid Misbahi,
Abdelali Kerbal,
Vincent Ferrières 
,
Daniel Plusquellec
,
Daniel Plusquellec
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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.