An efficient palladium-catalyzed C-O and subsequent C-C bond formation of 2,4-dichloroquinazoline have been described. The designed strategy results in the synthesis of novel 2-arylated quinazolin-4-ones framework with various aryl/heteroaryl boronic acids in moderate to good yields along with 2,4-diarylated quinazolines. This methodology offers a direct transformation of aryl halides to aryl alcohols/ketone as well as the straight forward application to generate a wide variety of monoaryl and diaryl quinazoline.
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Akkaoui A.E., 2010, Eur. J. Org. Chem, P862, DOI DOI 10.1002/EJOC.200900849