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DOI: 10.1055/a-2675-4145
Pd- and Photo-Promoted C−H Functionalizations of Phospholes
This work was supported by JSPS KAKENHI Grants JP 23K23345 [Grant-in-Aid for Scientific Research (B), to Koji Hirano], JP 25H02033 [Grant-in-Aid for Transformative Research Areas (A) (Publicly Offered Research), to Koji Hirano], JP 25K22257 [Grant-in-Aid for Challenging Research (Exploratory), to Koji Hirano], JST FOREST Program Grant JPMJFR211X to Koji Hirano, and Shanghai Pujiang Program (23PJ1411700) to Shibo Xu.
Supported by: Shanghai Pujiang Program 23PJ1411700
Supported by: Fusion Oriented REsearch for disruptive Science and Technology JPMJFR211X

Abstract
Significant research efforts have been devoted to the synthesis of substituted phospholes due to their exceptional optical and physical properties. In contrast to conventional methods, the direct C−H functionalizations of readily accessible phospholes offer an efficient and modular route to structurally diverse phosphole derivatives. In this account, we present our research group’s advancements in the regioselective C−H functionalizations of benzophospholes, including: (1) palladium-catalyzed C−H arylation, alkenylation, and alkynylation; (2) organophotoredox-catalyzed C−H alkoxycarbonylation, phosphinylation, and alkylation; and (3) related photo-promoted dehydrogenative cyclization and palladium-catalyzed annulative π-extension.
Keywords
Annulation - Benzophosphole - C−H functionalization - Heterocycles - Organophotocatalysis - Mallory reaction - Palladium catalysisPublication History
Received: 14 July 2025
Accepted after revision: 03 August 2025
Accepted Manuscript online:
03 August 2025
Article published online:
27 August 2025
© 2025. Thieme. All rights reserved.
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
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