Nickel‐Catalyzed <i>P</i> ‐Arylation of HP(= O)(R/OR) <sub>2</sub> Nucleophiles with (Hetero)Aryl Chlorides Enabled by DalPhos Ligation
Herein we disclose our development of broadly useful C-P cross-couplings of (hetero)aryl chlorides and HP(O)(R)<sub>2</sub> or HP(O)(OR)<sub>2</sub> nucleophiles, enabled by use of nickel/DalPhos-based catalysts. These typically use 5 mol% nickel at 110 °C for 18 hours, but the feasibility of shorter or milder reactions was demonstrated with one specific example. The ability to apply such transformations on gram scale, and in the P-arylation of active pharmaceutical ingredients (APIs) (i.e., chloroquine and clozapine) was also shown. Also described are our findings arising from the computational modelling of such cross-coupling reactions by use of density functional theory (DFT) calculations, which confirmed the clear preference for C-P bond formation involving three-centered reductive elimination through substrate P<sup>V</sup> pathways.
Authors
- David J. Nelson (ORCID: https://orcid.org/0000-0002-9461-5182)
- Catherine Weetman (ORCID: https://orcid.org/0000-0001-5643-9256)
- Mark Stradiotto (ORCID: https://orcid.org/0000-0002-6913-5160)
- Patrick DeRoy
- Michael J. Cotnam
- T. Kieran Redpath
Institutions
- Dalhousie University (CA)
- University of Strathclyde (GB)
- Paraza Pharma (Canada) (CA)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2025-09-15
- DOI
- https://doi.org/10.1002/chem.202502189
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- UK Research and Innovation
- Dalhousie University
- Natural Sciences and Engineering Research Council of Canada
- Engineering and Physical Sciences Research Council
- Natural Environment Research Council