Direct organocatalytic in situ generation of novel push-pull dienamines: Application in tandem Claisen-Schmidt/iso-aromatization reactions

Abstract

A new, green, regioselective, one-step, tandem reaction of an aldehyde possessing a non-enolizable carbonyl function with a highly substituted cyclohex-2-enone, under amine catalysis afforded highly substituted phenols or 2-arylidenecyclohexanones, respectively. The yields and regioselectivities were good. Evidence for a pathway involving formation of novel push-pull dienamines is presented along with examples demonstrating the amenability of the process to combinatorial chemistry. © 2005 Elsevier Ltd. All rights reserved.