Issue 11, 2016

A Cu-mediated one-pot Michael addition/α-arylation strategy using a diaryliodonium salt: a direct and efficient approach to α-aryl-β-substituted cyclic ketone scaffolds

Abstract

The direct and efficient construction of α-aryl-β-substituted cyclic ketone scaffolds has been achieved using a Cu-mediated one-pot Michael addition/α-arylation strategy. The reaction features easily available materials, broad substrate scope, moderate to good yield, and an excellent diastereoselectivity.

Graphical abstract: A Cu-mediated one-pot Michael addition/α-arylation strategy using a diaryliodonium salt: a direct and efficient approach to α-aryl-β-substituted cyclic ketone scaffolds

Supplementary files

Article information

Article type
Communication
Submitted
28 Nov 2015
Accepted
21 Dec 2015
First published
21 Dec 2015

Chem. Commun., 2016,52, 2382-2385

A Cu-mediated one-pot Michael addition/α-arylation strategy using a diaryliodonium salt: a direct and efficient approach to α-aryl-β-substituted cyclic ketone scaffolds

J. Pan, T. Chen, Z. Zhang, Y. Li, X. Zhang and F. Zhang, Chem. Commun., 2016, 52, 2382 DOI: 10.1039/C5CC09837H

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