Microwave-assisted synthesis of 2-acetyl-5-arylthiophenes and 4-(5-arylthiophen-2-yl)thiazoles via Suzuki coupling in water

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Abstract

2-Acetyl-5-bromothiophene and 4-(5-bromothiophen-2-yl)-2-methyl-1,3-thiazole, as deactivated bromide candidates, were prepared and used for Suzuki cross-coupling reactions with a number of aryl(hetaryl)boronic acids in water or DMF as solvents. The cross-coupling reactions were carried out under thermal heating as well as microwave irradiating conditions using a benzothiazole-based Pd(II)-precatalyst. Optimization of the catalytic reaction condition was also studied.

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Dawood, K. M., Elamin, M. B., & Farag, A. M. (2015). Microwave-assisted synthesis of 2-acetyl-5-arylthiophenes and 4-(5-arylthiophen-2-yl)thiazoles via Suzuki coupling in water. Arkivoc, 2015(7), 50–62. https://doi.org/10.3998/ark.5550190.p009.018

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