Issue 24, 2016

Direct conjugate alkylation of α,β-unsaturated carbonyls by TiIII-catalysed reductive umpolung of simple activated alkenes

Abstract

The titanium(III)-catalysed cross-selective reductive umpolung of Michael-acceptors represents a unique direct conjugate β-alkylation reaction. It allows the cross-selective preparation of 1,6- and 1,4-difunctionalised building blocks without the requirement of stoichiometric organometallic reagents. In this full paper, the development and scope of the titanium(III)-catalysed cross-selective reductive umpolung of Michael-acceptors is described. Based on the observed selectivities and additional mechanistic experiments a refined mechanistic proposal is presented.

Graphical abstract: Direct conjugate alkylation of α,β-unsaturated carbonyls by TiIII-catalysed reductive umpolung of simple activated alkenes

  • This article is part of the themed collection: New Talent

Supplementary files

Article information

Article type
Paper
Submitted
22 Dec 2015
Accepted
15 Jan 2016
First published
25 Jan 2016
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2016,14, 5673-5682

Direct conjugate alkylation of α,β-unsaturated carbonyls by TiIII-catalysed reductive umpolung of simple activated alkenes

P. Bichovski, T. M. Haas, M. Keller and J. Streuff, Org. Biomol. Chem., 2016, 14, 5673 DOI: 10.1039/C5OB02631H

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