6909-26-8Relevant articles and documents
Studies towards the taming of the 'carbocation' in the regioselective ring opening of epoxides to allylic alcohols
Chapman, Helen A.,Herbal, Karim,Motherwell, William B.
experimental part, p. 595 - 598 (2010/09/15)
Regioselective isomerisation of epoxides to allylic alcohols can be achieved using p-toluenesulfonic acid in the presence of 1,3- dimethylimidazolidin-2-one. Georg Thieme Verlag Stuttgart.
ELECTROCHEMICAL PROCEDURE DIRECTED TO THE SELECTIVE RING OPENING OF EPOXIDES TO ALLYLIC ALCOHOLS
Uneyama, Kenji,Nisiyama, Noriyuki,Torii, Sigeru
, p. 4137 - 4138 (2007/10/02)
A transformation of epoxides 2 into allylic alcohols 1 was achieved by an electrogenerated acid-catalysis in ClCH2CH2Cl - TsONa - TsONEt4 - Pt system.