Organophotoredox-Catalyzed C–H Functionalizations of Benzophospholes
Surface Modification
Rose bengal
DOI:
10.1021/acs.orglett.4c01535
Publication Date:
2024-06-18T16:24:47Z
AUTHORS (4)
ABSTRACT
An organophotoredox-catalyzed oxidative C-H functionalization of benzophospholes has been developed. The alkoxycarbonylation with methyl carbazate occurs in the presence Rose bengal, whereas Eosin Y enables dehydrogenative coupling secondary phosphine oxides and ethers, delivering phosphinylated alkylated products. scope partners is complementary to that conventional metal-promoted activation, thus successfully expanding chemical space substituted phospholes accessed by protocols.
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