Chemodivergent phosphonylation of diazocarboxylates: light-on vs . light-off reactions
By tapping into the divergent reactivity of diazocarboxylates under thermal and photocatalytic conditions, we could develop chemodivergent phosphonylation protocols for α-diazocarboxylates with trialkyl phosphites. While the thermal reaction led to N-P bond formation affording phosphonylated hydrazo...
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Veröffentlicht in: | Organic & biomolecular chemistry 2024-06, Vol.22 (25), p.5224-5228 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | By tapping into the divergent reactivity of diazocarboxylates under thermal and photocatalytic conditions, we could develop chemodivergent phosphonylation protocols for α-diazocarboxylates with trialkyl phosphites. While the thermal reaction led to N-P bond formation affording phosphonylated hydrazones, the visible light-mediated reaction furnished phosphonylated aryl carboxylates through C-P bond formation. Both reactions are notable for their operational simplicity and mild conditions affording products in good yields without the requirement of a metal, base or photocatalyst. |
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ISSN: | 1477-0520 1477-0539 1477-0539 |
DOI: | 10.1039/d4ob00573b |