Issue 5, 2003

Pd-catalysed cross coupling of terminal alkynes to diynes in the absence of a stoichiometric additive

Abstract

An efficient, room temperature procedure for the cross-coupling of a range of terminal alkynes, using standard Sonogashira cross-coupling conditions (Pd/Cu) is presented. At higher reaction temperatures, head-to-tail or head-to-head dimerisation affords 1,3- and 1,4-disubstituted enynes, respectively as minor products.

Graphical abstract: Pd-catalysed cross coupling of terminal alkynes to diynes in the absence of a stoichiometric additive

Article information

Article type
Communication
Submitted
18 Dec 2002
Accepted
24 Jan 2003
First published
07 Feb 2003

Chem. Commun., 2003, 632-633

Pd-catalysed cross coupling of terminal alkynes to diynes in the absence of a stoichiometric additive

I. J. S. Fairlamb, P. S. Bäuerlein, L. R. Marrison and J. M. Dickinson, Chem. Commun., 2003, 632 DOI: 10.1039/B212430K

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