39067-97-5Relevant academic research and scientific papers
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.
, p. 595 - 598 (2010)
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.
