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June 1, 2026The Journal of Organic Chemistry0 citations

Paired Electrolysis-Driven P(O)–N Bond Formation via Reductive Cross-Coupling of Nitroarenes with Phosphine Oxides

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ZDZhaojun DingJWJingjing WenXLXiyu Luo

Key Points

  • This research aims to develop an efficient method for forming P(O)-N bonds using paired electrolysis in organic synthesis.
  • Utilized paired electrolysis-promoted reductive cross-coupling reactions without metal catalysts or chemical reductants.
  • Synthesis involved nitroarenes and phosphine oxides to create phosphinamides, phosphonamides, and phosphoramides.
  • Investigated mechanistic pathways including radical and Atherton-Todd pathways.
  • P(O)-N bonds formed efficiently with broad functional group compatibility.
  • Chemo-selective P(O)-N bond formation characterized by radical involvement and various product types.

Abstract

The efficient construction of the P(O)-N bond is crucial in organic synthesis. P(O)-N bond formations with nitroarenes and phosphine oxides were accomplished via paired electrolysis-promoted reductive cross-coupling reactions under metal-catalyst- and chemical-reductant-free conditions. The combination of paired electrolysis with reductive coupling enabled P(O)-N bond formation in a chemo-selective fashion and exhibited broad functional group tolerance, which allows for the synthesis of phosphinamides, phosphonamides, and phosphoramides and provides access to late-stage functionalization. Mechanistic studies indicated that both radical and Atherton-Todd pathways are operative in the electro-reductive coupling.

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Cite This Study

Ding et al. (2026) studied this question.

synapsesocial.com/papers/6a1d218f02fbce91306377d2https://doi.org/10.1021/acs.joc.5c03082
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