Phototriggered Self-Catalyzed\nPhosphorylation of 3,4-Dihydroquinoxalin-2(1<i>H</i>)‑ones\nwith Diarylphosphine Oxides in EtOH

A highly effective external photocatalyst- and additive-free\nmethod\nfor the phosphorylation of 3,4-dihydroquinoxalin-2(1<i>H</i>)-ones to produce phosphorylated dihydroquinoxalin-2(1<i>H</i>)-ones has been reported. A wide variety of phosphorylated products\nwere formed in good to excellent yields. Preliminary mechanistic studies\nreveal that the phosphorylation process involves an EnT process, a\nSET process, a HAT process, and a deprotonation process.

Publication Details

Journal
Figshare
Published
2024-09-19
DOI
https://doi.org/10.1021/acs.joc.4c01184.s001
Primary Topic
Organophosphorus compounds synthesis
Type
article
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article

Phototriggered Self-Catalyzed\nPhosphorylation of 3,4-Dihydroquinoxalin-2(1H)‑ones\nwith Diarylphosphine Oxides in EtOH

Figshare
Organophosphorus compounds synthesis
article

Phototriggered Self-Catalyzed\nPhosphorylation of 3,4-Dihydroquinoxalin-2(1H)‑ones\nwith Diarylphosphine Oxides in EtOH

article en

Abstract

A highly effective external photocatalyst- and additive-free\nmethod\nfor the phosphorylation of 3,4-dihydroquinoxalin-2(1<i>H</i>)-ones to produce phosphorylated dihydroquinoxalin-2(1<i>H</i>)-ones has been reported. A wide variety of phosphorylated products\nwere formed in good to excellent yields. Preliminary mechanistic studies\nreveal that the phosphorylation process involves an EnT process, a\nSET process, a HAT process, and a deprotonation process.

Figshare
Openalex Percentile: Top 73%
Organophosphorus compounds synthesis
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Phototriggered Self-Catalyzed\nPhosphorylation of 3,4-Dihydroquinoxalin-2(1<i>H</i>)‑ones\nwith Diarylphosphine Oxides in EtOH · Figshare (2024) | TGRS Research Map | TGRS