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

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

Youssef Kabriemail, Pierre Verhaegheemail, Armand Gellisemail and Patrice Vanelle* email
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; in revised form: 8 April 2010 / Accepted: 21 April 2010 / Published: 27 April 2010
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Abstract: 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

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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.

AMA 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(5):2949-2961.

Chicago/Turabian Style

Kabri, Youssef; Verhaeghe, Pierre; Gellis, Armand; Vanelle, Patrice. 2010. "Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines." Molecules 15, no. 5: 2949-2961.

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