The bioinspired design of a reagent allows the functionalization of Cα–H of α,β-unsaturated carbonyl compounds via the Baylis–Hillman chemistry under ambient conditions†
Palwinder Singh,Arun Kumar,Sukhmeet Kaur,Jagroop Kaur,Harpreet Singh
Chemical Communications Pub Date : 01/11/2016 00:00:00 , DOI:10.1039/C5CC08830E
Abstract

A rationally designed reagent capable of affecting alkylation at Cα of α,β-unsaturated carbonyl compounds is reported. The reaction proceeded at room temperature without any additives. The pH and H-bond formation during the reaction play a key role in the working of the reagent.

Graphical abstract: The bioinspired design of a reagent allows the functionalization of Cα–H of α,β-unsaturated carbonyl compounds via the Baylis–Hillman chemistry under ambient conditions