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    Iridium (I)-Catalyzed Enantioselective Hydroarylation of Alkenes via C-H bond Activation: Experiment and Computation.

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    Name:
    Cchem.202001793.pdf
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    1.505Mb
    Format:
    PDF
    Description:
    Accepted manuscript
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    Type
    Article
    Authors
    Rueping, Magnus cc
    Shinde, Valmik cc
    Mane, Manoj Vasisht cc
    Cavallo, Luigi cc
    KAUST Department
    Chemical Science Program
    KAUST Catalysis Center (KCC)
    King Abdullah University of Science and Technology, KAUST Catalysis Center, Landoltweg 1, 23955, Thuwal, SAUDI ARABIA.
    Physical Science and Engineering (PSE) Division
    Date
    2020-06-22
    Online Publication Date
    2020-06-22
    Print Publication Date
    2020-07-02
    Embargo End Date
    2021-04-18
    Submitted Date
    2020-04-15
    Permanent link to this record
    http://hdl.handle.net/10754/662584
    
    Metadata
    Show full item record
    Abstract
    A new catalytic enantioselective hydroarylation of unactivated olefins provides rapid access to functionalized chiral dihydrobenzofurans with good yields and excellent enantio-selectivities. Simple aromatic ketones or amides act as directing group allowing the regioselective reaction at the more hindered ortho position. Tertiary benzylic stereocenters are obtained directly under mild reaction conditions and with complete atom economy from readily available starting materials.
    Citation
    Rueping, M., Shinde, V., Mane, M., & Cavallo, L. (2020). Iridium (I)-Catalyzed Enantioselective Hydroarylation of Alkenes via C–H bond Activation: Experiment and Computation. Chemistry – A European Journal. doi:10.1002/chem.202001793
    Publisher
    Wiley
    Journal
    Chemistry – A European Journal
    DOI
    10.1002/chem.202001793
    PubMed ID
    32301132
    Additional Links
    https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.202001793
    Relations
    Is Supplemented By:
    • [Dataset]
      Shinde, Valmik. (2018). CCDC 1877011: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/CCDC.CSD.CC2105R0. DOI: 10.5517/ccdc.csd.cc2105r0 Handle: 10754/665102
    ae974a485f413a2113503eed53cd6c53
    10.1002/chem.202001793
    Scopus Count
    Collections
    Articles; Physical Science and Engineering (PSE) Division; Chemical Science Program; KAUST Catalysis Center (KCC)

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