Photoelectrocatalyzed Alkylation of Phosphonites by Direct Decarboxylative C(sp<sup>3</sup>)‐P Coupling

Abstract A photoelectrocatalytic method is presented that achieves direct decarboxylative C(sp 3 )‐P coupling, providing a modular route to alkylphosphinates and alkylphosphonates from readily available carboxylic acids. The success of this reaction hinges on the synergistic combination of electrochemical anodic oxidation and photocatalytic ligand to metal charge transfer (LMCT) decarboxylation. By employing P(III) reagents as limiting reagents, our approach enables efficient alkyl modification of medicinally important nucleosides and complex molecules derived phosphonites, which were challenging to access by existing methods. Detailed mechanistic studies elucidate the critical roles of Fe catalysts and additives, offering valuable insights into the reaction pathway and laying the foundation for future advancements in photoelectrocatalytic C(sp 3 )‐heteroatom bond‐forming reactions.

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Publication Details

Journal
Angewandte Chemie
Published
2025-01-27
DOI
https://doi.org/10.1002/ange.202500744
Citations
1
Primary Topic
Organophosphorus compounds synthesis
Type
article
Field-Weighted Citation Impact
0.94
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article

Photoelectrocatalyzed Alkylation of Phosphonites by Direct Decarboxylative C(sp3)‐P Coupling

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1 citations
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article

Photoelectrocatalyzed Alkylation of Phosphonites by Direct Decarboxylative C(sp3)‐P Coupling

Tian Xie, Dali Wang, Ming Shan, Jia-Bao Wang, Keyong Yuan
article en
1 citations

Abstract

Abstract A photoelectrocatalytic method is presented that achieves direct decarboxylative C(sp 3 )‐P coupling, providing a modular route to alkylphosphinates and alkylphosphonates from readily available carboxylic acids. The success of this reaction hinges on the synergistic combination of electrochemical anodic oxidation and photocatalytic ligand to metal charge transfer (LMCT) decarboxylation. By employing P(III) reagents as limiting reagents, our approach enables efficient alkyl modification of medicinally important nucleosides and complex molecules derived phosphonites, which were challenging to access by existing methods. Detailed mechanistic studies elucidate the critical roles of Fe catalysts and additives, offering valuable insights into the reaction pathway and laying the foundation for future advancements in photoelectrocatalytic C(sp 3 )‐heteroatom bond‐forming reactions.

Angewandte ChemieVol. 137(15)
Shanghai Jiao Tong University (CN), Shanghai Advanced Research Institute (CN)
Openalex Percentile: Top 30%
Organophosphorus compounds synthesis
0.94
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