Ligand-Enabled Gold-Catalyzed C–P Cross-Coupling Reactions

Herein, we report a ligand-enabled gold-catalyzed C(sp2)–P cross-coupling of aryl iodides with phosphine oxides to afford triaryl phosphine oxides. The success of this transformation relies on two factors: the crucial role of silver salts in preventing catalyst deactivation through Ag–phosphine oxide complex formation and the use of masked phosphinylating agents. Detailed mechanistic investigations including several control experiments, HRMS analysis, 31P NMR, and DFT studies have been performed to underpin the mechanism.

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Publication Details

Journal
ACS Catalysis
Published
2025-11-10
DOI
https://doi.org/10.1021/acscatal.5c06748
Citations
2
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
1.87
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article

Ligand-Enabled Gold-Catalyzed C–P Cross-Coupling Reactions

Nitin T. Patil, Manoj V. Mane, Urvashi Urvashi, Nisha Nisha
2 citations
ACS Catalysis
Catalytic Alkyne Reactions
1.87
article

Ligand-Enabled Gold-Catalyzed C–P Cross-Coupling Reactions

Nitin T. Patil, Manoj V. Mane, Urvashi Urvashi, Nisha Nisha
article en
2 citations

Abstract

Herein, we report a ligand-enabled gold-catalyzed C(sp2)–P cross-coupling of aryl iodides with phosphine oxides to afford triaryl phosphine oxides. The success of this transformation relies on two factors: the crucial role of silver salts in preventing catalyst deactivation through Ag–phosphine oxide complex formation and the use of masked phosphinylating agents. Detailed mechanistic investigations including several control experiments, HRMS analysis, 31P NMR, and DFT studies have been performed to underpin the mechanism.

ACS CatalysisVol. 15(22)
Jain University (IN), Indian Institute of Science Education and Research, Bhopal (IN)
Openalex Percentile: Top 13%
Catalytic Alkyne Reactions
1.87
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