A Regioselective Aluminum Chloride-catalyzed Acylation of Allylic Selenides via α-Silyl Intermediates. A Facile Route to Dihydrojasmone
作者:Kunio Hiroi、Hiroyasu Sato
DOI:10.1246/cl.1986.1723
日期:1986.10.5
The aluminum chloride-catalyzed acylation of α-silylallylic selenides with acid chlorides at −78 °C produced γ-acylated vinylic selenides regioselectively. α-Silylallylic selenides in some cases underwent [1,3] shifts of the selenenyl groups by the catalysis with aluminum chloride, affording γ-silylallylic selenides. This regioselective acylation of allylic selenides provides a new route to dihydrojasmone