A Nickel Pre-Catalyst for the O -Arylation of Primary, Secondary, and Tertiary Alcohols with (Hetero)aryl Chlorides
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.
Authors
- Mark Stradiotto (ORCID: https://orcid.org/0000-0002-6913-5160)
- Patrick DeRoy
- Emily C. Jackson (ORCID: https://orcid.org/0000-0002-2537-7387)
- Katherine N. Robertson (ORCID: https://orcid.org/0000-0002-5602-8059)
- Peter L. Fox (ORCID: https://orcid.org/0009-0009-3345-9292)
- Kathleen M. Morrison
- Erika M. H. Elliott
Institutions
- Dalhousie University (CA)
- University of Saint Mary (US)
- Paraza Pharma (Canada) (CA)
- Saint Mary's University of Minnesota (US)
Publication Details
- Journal
- Organometallics
- Published
- 2026-09-25
- DOI
- https://doi.org/10.1021/acs.organomet.6c00313
- Citations
- 1
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 2.19