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

Received: 24 March 2010; in revised form: 8 April 2010 / Accepted: 21 April 2010 / Published: 27 April 2010
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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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