Synlett
DOI: 10.1055/a-2675-4145
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Pd- and Photo-Promoted C−H Functionalizations of Phospholes

Shibo Xu
1   School of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai, China (Ringgold ID: RIN92263)
,
2   Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Osaka, Japan
3   Innovative Catalysis Science Division, Institute for Open and Transdisciplinary Research Initiatives (ICS-OTRI), Osaka University, Osaka, Japan
› Author Affiliations

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


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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.



Publication History

Received: 14 July 2025

Accepted after revision: 03 August 2025

Accepted Manuscript online:
03 August 2025

Article published online:
27 August 2025

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