Nickel-CatalyzedDecarbonylationof Aromatic CarboxylicAcids with P(O)‑H<sub>(2)</sub> Compounds to Form C–PBonds

A novel strategy for C–P bond formation has been developed. The reaction employed aromatic carboxylic acids as the source of aromatic groups to couple with three types of P(O)-H<sub>(2)</sub> compounds without the need to isolate intermediates, thereby achieving a one-pot construction of carbon–phosphorus bonds. The protocol demonstrated excellent applicability and functional group tolerance, enabling the production of Ar–P(O)R<sub>2</sub> and Ar<sub>2</sub>–PPh with moderate to excellent yields.

Publication Details

Journal
Figshare
Published
2025-02-20
DOI
https://doi.org/10.1021/acs.joc.4c02554.s001
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
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article

Nickel-CatalyzedDecarbonylationof Aromatic CarboxylicAcids with P(O)‑H(2) Compounds to Form C–PBonds

Figshare
Catalytic Cross-Coupling Reactions
article

Nickel-CatalyzedDecarbonylationof Aromatic CarboxylicAcids with P(O)‑H(2) Compounds to Form C–PBonds

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Abstract

A novel strategy for C–P bond formation has been developed. The reaction employed aromatic carboxylic acids as the source of aromatic groups to couple with three types of P(O)-H<sub>(2)</sub> compounds without the need to isolate intermediates, thereby achieving a one-pot construction of carbon–phosphorus bonds. The protocol demonstrated excellent applicability and functional group tolerance, enabling the production of Ar–P(O)R<sub>2</sub> and Ar<sub>2</sub>–PPh with moderate to excellent yields.

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Openalex Percentile: Top 69%
Catalytic Cross-Coupling Reactions
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Nickel-CatalyzedDecarbonylationof Aromatic CarboxylicAcids with P(O)‑H<sub>(2)</sub> Compounds to Form C–PBonds · Figshare (2025) | TGRS Research Map | TGRS