Abstract
A range of novel 4-amino-6-arylpyrimidines has been prepared under mild conditions by an electrochemical reductive cross-coupling between 4-amino-6-chloropyrimidines and functionalized aryl halides. The process, which employs a sacrificial iron anode in conjunction with a nickel(II) catalyst, allows the formation of coupling products in moderate to high yields. © 2011 by the authors; licensee MDPI, Basel, Switzerland.
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Sengmany, S., Le Gall, E., & Léonel, E. (2011). An electrochemical synthesis of functionalized arylpyrimidines from 4-Amino-6-Chloropyrimidines and aryl halides. Molecules, 16(7), 5550–5560. https://doi.org/10.3390/molecules16075550
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