Issue 75, 2012

Caryl–Calkyl bond formation from Cu(ClO4)2-mediated oxidative cross coupling reaction between arenes and alkyllithium reagents through structurally well-defined Ar–Cu(iii) intermediates

Abstract

The stable and structurally well-defined Ar–Cu(III) intermediates, that are prepared almost quantitatively from the reaction of azacalix[1]arene[3]pyridines with Cu(ClO4)2·6H2O under aerobic conditions, reacted smoothly with a number of alkyllithium reagents under mild conditions to form Caryl–Calkyl bonds.

Graphical abstract: Caryl–Calkyl bond formation from Cu(ClO4)2-mediated oxidative cross coupling reaction between arenes and alkyllithium reagents through structurally well-defined Ar–Cu(iii) intermediates

Supplementary files

Article information

Article type
Communication
Submitted
16 Jul 2012
Accepted
01 Aug 2012
First published
03 Aug 2012

Chem. Commun., 2012,48, 9418-9420

Caryl–Calkyl bond formation from Cu(ClO4)2-mediated oxidative cross coupling reaction between arenes and alkyllithium reagents through structurally well-defined Ar–Cu(III) intermediates

Z. Wang, L. Zhao and M. Wang, Chem. Commun., 2012, 48, 9418 DOI: 10.1039/C2CC35067J

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