We describe here an efficient ruthenium-catalyzed C–H bond ortho-arylation of 9-(pyrimidin-2-yl)-9H-carbazole by using boronic acids. This methodology exhibits excellent and high site-selectivity, functional group tolerance and was found to give the desired product in moderate to good yields.
K. Harsha Vardhan Reddy, R. U. Kumar, V. P. Reddy, G. Satish, J. B. Nanubolu and Y. V. D. Nageswar, RSC Adv., 2016, 6, 54431 DOI: 10.1039/C6RA09825H
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