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Regioselective Suzuki-Miyaura reaction: Application to the microwave-promoted synthesis of 4,7-diarylquinazolines

Molecules (2010) 15(5) 2949-2961
DOI: 10.3390/molecules15052949
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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. © 2010 by the authors.

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APA

Kabri, Y., Verhaeghe, P., Gellis, A., & Vanelle, P. (2010). Regioselective Suzuki-Miyaura reaction: Application to the microwave-promoted synthesis of 4,7-diarylquinazolines. Molecules, 15(5), 2949–2961. https://doi.org/10.3390/molecules15052949

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