Issue 6, 2013

Access to congested quaternary centers by Pd-catalyzed intermolecular γ-arylation of unactivated α,β-unsaturated aldehydes

Abstract

A palladium-catalyzed intermolecular γ-arylation of γ-branched α,β-unsaturated aldehydes has been developed. The reaction allows congested quaternary centers to be forged on a remote position from the carbonyl group, affording a variety of products in high yield and with consistently high stereoselectivity using very low catalyst loadings. The synthetic utility of the products has been highlighted by a series of derivatizations and the potential of the method to be extended to remote ε-functionalization has been demonstrated.

Graphical abstract: Access to congested quaternary centers by Pd-catalyzed intermolecular γ-arylation of unactivated α,β-unsaturated aldehydes

Supplementary files

Article information

Article type
Edge Article
Submitted
25 Mar 2013
Accepted
17 Apr 2013
First published
17 Apr 2013

Chem. Sci., 2013,4, 2619-2624

Access to congested quaternary centers by Pd-catalyzed intermolecular γ-arylation of unactivated α,β-unsaturated aldehydes

I. Franzoni, L. Guénée and C. Mazet, Chem. Sci., 2013, 4, 2619 DOI: 10.1039/C3SC50806D

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