A Nickel Pre-Catalyst for the O -Arylation of Primary, Secondary, and Tertiary Alcohols with (Hetero)aryl Chlorides
Abstract
Abstract While base metal-catalyzed cross-couplings of alcohols and (hetero)aryl chlorides have emerged over the past decade, the development of a single pre-catalyst capable of promoting such transformations spanning all of primary, secondary, and tertiary (aliphatic) alcohols remains an enduring challenge. Herein we disclose the easily prepared, air-stable 4-cyanophenyl pre-catalyst (L2)Ni(4-CN-Ph)Cl (L2 = CgPhen-DalPhos), which is shown to be capable of promoting, with useful reaction scope, the C–O cross-coupling of all such alcohol classes with (hetero)aryl chlorides.
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Authors: Emily C. Jackson, Erika M. H. Elliott, Kathleen M. Morrison, Peter L. Fox, Katherine N. Robertson, Patrick DeRoy, Mark Stradiotto
Institutions: Dalhousie University, Saint Mary's University of Minnesota, University of Saint Mary, Paraza Pharma (Canada)