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Molecules 2010, 15(5), 2949-2961; doi:10.3390/molecules15052949

Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines

Laboratoire de Pharmacochimie Radicalaire, Faculté de Pharmacie, Universités d’Aix-Marseille I, II et III - UMR CNRS 6264 , Laboratoire Chimie Provence, 27 Boulevard Jean Moulin, 13385 Marseille cedex 05, France
Author to whom correspondence should be addressed.
Received: 24 March 2010 / Revised: 8 April 2010 / Accepted: 21 April 2010 / Published: 27 April 2010
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New diarylquinazolines displaying pharmaceutical potential were synthesized in high yields from 4,7-dichloro-2-(2-methylprop-1-enyl)-6-nitroquinazoline by using microwave-promoted regioselective Suzuki-Miyaura cross-coupling reactions.
Keywords: quinazoline; Suzuki-Miyaura reaction; microwaves; SRN1 quinazoline; Suzuki-Miyaura reaction; microwaves; SRN1

This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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MDPI and ACS Style

Kabri, Y.; Verhaeghe, P.; Gellis, A.; Vanelle, P. Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines. Molecules 2010, 15, 2949-2961.

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