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.

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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

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article

Nickel‐Catalyzed P ‐Arylation of HP(= O)(R/OR) 2 Nucleophiles with (Hetero)Aryl Chlorides Enabled by DalPhos Ligation

David J. Nelson, Catherine Weetman, Mark Stradiotto, Patrick DeRoy et al.
Chemistry - A European Journal
Catalytic C–H Functionalization Methods
article

Nickel‐Catalyzed P ‐Arylation of HP(= O)(R/OR) 2 Nucleophiles with (Hetero)Aryl Chlorides Enabled by DalPhos Ligation

David J. Nelson, Catherine Weetman, Mark Stradiotto, Patrick DeRoy, Michael J. Cotnam, T. Kieran Redpath
article en

Abstract

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.

Chemistry - A European JournalVol. 31(59)
Dalhousie University (CA), University of Strathclyde (GB), Paraza Pharma (Canada) (CA)
UK Research and Innovation, Dalhousie University, Natural Sciences and Engineering Research Council of Canada, Engineering and Physical Sciences Research Council, Natural Environment Research Council
Openalex Percentile: Top 81%
Catalytic C–H Functionalization Methods
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