Photoredox-catalyzed decarboxylative alkylation/cyclization of alkynylphosphine oxides: a metal- and oxidant-free method for accessing benzo[]phosphole oxides
By photoredox-catalysis, alkylation/aryl C-H cyclization of readily available alkynylphosphine oxides towards benzo[ b ]phospholes has been realized under metal- and oxidant-free conditions at room temperature. This reaction readily incorporates various functionalized alkyl groups into the benzo[ b...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2019, Vol.55 (2), p.233-236 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | By photoredox-catalysis, alkylation/aryl C-H cyclization of readily available alkynylphosphine oxides towards benzo[
b
]phospholes has been realized under metal- and oxidant-free conditions at room temperature. This reaction readily incorporates various functionalized alkyl groups into the benzo[
b
]phosphole skeletons, representing a mild and versatile tool for the preparation of valuable phosphole compounds.
By photoredox-catalysis, alkylation/aryl cyclization of alkynylphosphine oxides towards benzo[
b
]phospholes has been realized under metal- and oxidant-free conditions at room temperature. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c8cc08689c |