Reduction of .BETA.-keto sulfoxides having an alkyl group and a chlorine atom on the .ALPHA.-carbon. A synthesis of (E)-.ALPHA.,.BETA.-epoxy sulfoxides.
- 1 January 1989
- journal article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 37 (1) , 184-186
- https://doi.org/10.1248/cpb.37.184
Abstract
Oxidation of the chlorohydrins derived from 1-chloroalkyl phenyl sulfoxides and aldehydes gave the β-keto sulfoxides having an alkyl group and a chlorine atom on the α-carbon. The β-keto sulfoxides were reduced with diisobutylaluminum hydride to afford the syn-chlorohydrins as sole products, which were converted to the (E)-α, β-epoxy sulfoxides.Keywords
This publication has 0 references indexed in Scilit: