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Development of a palladium-catalyzed α-arylation of cyclopropyl nitriles. | LitMetric

Development of a palladium-catalyzed α-arylation of cyclopropyl nitriles.

Org Lett

Department of Process Chemistry, Merck Research Laboratories , 2000 Galloping Hill Road, Kenilworth, New Jersey 07033, United States.

Published: December 2014

1,1-Disubstituted aryl cyclopropyl nitriles are useful moieties in biologically active compounds and provide access to a range of cyclopropyl derivatives. Herein, we describe the development of a palladium-catalyzed α-arylation of cyclopropyl, cyclobutyl, and cyclopentyl nitriles that affords these functional groups in one step from a variety of aryl bromides in good to excellent yields. Furthermore, we demonstrate the transformation of aryl cyclopropyl nitriles into aryl trifluoromethyl cyclopropanes.

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Source
http://dx.doi.org/10.1021/ol5030426DOI Listing

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