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    Advances in allylic and benzylic C–H bond functionalization enabled by metallaphotoredox catalysis

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    d1cc06285a.pdf
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    PDF
    Description:
    Accepted manuscript
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    Type
    Article
    Authors
    Yue, Huifeng cc
    Zhu, Chen cc
    Huang, Long
    Dewanji, Abhishek
    Rueping, Magnus cc
    KAUST Department
    KAUST Catalysis Center (KCC)
    Chemical Science Program
    Physical Science and Engineering (PSE) Division
    KAUST Grant Number
    URF/1/4384
    Date
    2022
    Online Publication Date
    2021-12-06
    Permanent link to this record
    http://hdl.handle.net/10754/673992
    
    Metadata
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    Abstract
    Metallaphoto-catalysis has been established as a robust platform for efficient construction of a range of chemical bonds. Moreover, transformation of native functionalities such as C(sp3)–H bonds to produce functional molecules represents one of the most attractive strategies in organic synthesis. Merging two powerful methodologies, metallaphoto-catalyzed benzylic and allylic C(sp3)–H bond functionalizations provide a series of general and mild approaches for diversification of alkylbenzenes and alkenes.
    Citation
    Yue, H., Zhu, C., Huang, L., Dewanji, A., & Rueping, M. (2022). Advances in allylic and benzylic C–H bond functionalization enabled by metallaphotoredox catalysis. Chemical Communications. doi:10.1039/d1cc06285a
    Sponsors
    This work was financially supported by the King Abdullah University of Science and Technology (KAUST), Saudi Arabia, Office of Sponsored Research (URF/1/4384).
    Publisher
    Royal Society of Chemistry (RSC)
    Journal
    Chemical Communications
    DOI
    10.1039/d1cc06285a
    Additional Links
    http://xlink.rsc.org/?DOI=D1CC06285A
    ae974a485f413a2113503eed53cd6c53
    10.1039/d1cc06285a
    Scopus Count
    Collections
    Articles; Physical Science and Engineering (PSE) Division; Chemical Science Program; KAUST Catalysis Center (KCC)

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