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    Nickel-catalyzed exo-selective hydroacylation/Suzuki cross-coupling reaction.

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    Manuscript-revised_.pdf
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    PDF
    Description:
    Accepted manuscript
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    Type
    Article
    Authors
    Lee, Shao-Chi
    Guo, Lin
    Rueping, Magnus cc
    KAUST Department
    Chemical Science Program
    KAUST Catalysis Center (KCC)
    Physical Science and Engineering (PSE) Division
    Date
    2019
    Embargo End Date
    2020-11-29
    Permanent link to this record
    http://hdl.handle.net/10754/660487
    
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    Abstract
    The first nickel-catalyzed intramolecular hydroacylation/Suzuki cross coupling cascade of o-allylbenzaldehydes with a broad range of phenylboronic acid neopentyl glycol esters has been developed. This strategy shows high regioselectivity and step economy in the construction of two C-C bonds via aldehyde C-H bond activation, affording valuable indanones with high efficiency.
    Citation
    Lee, S.-C., Guo, L., & Rueping, M. (2019). Nickel-catalyzed exo-selective hydroacylation/Suzuki cross-coupling reaction. Chemical Communications. doi:10.1039/c9cc07558e
    Publisher
    Royal Society of Chemistry (RSC)
    Journal
    Chemical communications (Cambridge, England)
    DOI
    10.1039/c9cc07558e
    Additional Links
    http://xlink.rsc.org/?DOI=C9CC07558E
    ae974a485f413a2113503eed53cd6c53
    10.1039/c9cc07558e
    Scopus Count
    Collections
    Articles; Physical Science and Engineering (PSE) Division; Chemical Science Program; KAUST Catalysis Center (KCC)

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