• Login
    View Item 
    •   Home
    • Research
    • Articles
    • View Item
    •   Home
    • Research
    • Articles
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Browse

    All of KAUSTCommunitiesIssue DateSubmit DateThis CollectionIssue DateSubmit Date

    My Account

    Login

    Quick Links

    Open Access PolicyORCID LibguideTheses and Dissertations LibguideSubmit an Item

    Statistics

    Display statistics

    Reactivity in Nickel Catalyzed Multicomponent Sequential Reductive Cross-Coupling Reactions

    • CSV
    • RefMan
    • EndNote
    • BibTex
    • RefWorks
    Thumbnail
    Name:
    Angew Chem Int Ed - 2022 - Chen - Reactivity in Nickel Catalyzed Multicomponent Sequential Reductive Cross‐Coupling.pdf
    Size:
    1.446Mb
    Format:
    PDF
    Description:
    Accepted Manuscript
    Embargo End Date:
    2023-06-21
    Download
    Type
    Article
    Authors
    Chen, Haifeng
    Yue, Huifeng
    Zhu, Chen cc
    Rueping, Magnus cc
    KAUST Department
    King Abdullah University of Science and Technology KAUST Catalysis Center Chemical Science Program SAUDI ARABIA
    KAUST Catalysis Center (KCC)
    Physical Science and Engineering (PSE) Division
    Chemical Science Program
    Date
    2022-06-21
    Embargo End Date
    2023-06-21
    Permanent link to this record
    http://hdl.handle.net/10754/679245
    
    Metadata
    Show full item record
    Abstract
    A nickel-catalyzed three-component reductive carbonylation of alkyl halides, aryl halides, and ethyl chloroformate is described. Ethyl chloroformate is utilized as a safe and readily available source of CO in this multi-component protocol, providing an efficient and practical alternative for the synthesis of aryl-alkyl ketones. The reaction exhibits a wide substrate scope and good functional group compatibility. Experimental and DFT mechanistic studies highlight the complexity the cross-electrophile coupling and provide insight into the sequence of the three consecutive oxidative additions of aryl halide, chloroformate and akyl halide.
    Citation
    Chen, H., Yue, H., Zhu, C., & Rueping, M. (2022). Reactivity in Nickel Catalyzed Multicomponent Sequential Reductive Cross-Coupling Reactions. Angewandte Chemie International Edition. Portico. https://doi.org/10.1002/anie.202204144
    Sponsors
    The authors thank the King Abdullah University of Science and Technology (KAUST) for financial support and the KAUST Supercomputing Laboratory for providing the computational resources of the Shaheen II supercomputer.
    Publisher
    Wiley
    Journal
    Angewandte Chemie International Edition
    DOI
    10.1002/anie.202204144
    Additional Links
    https://onlinelibrary.wiley.com/doi/10.1002/anie.202204144
    ae974a485f413a2113503eed53cd6c53
    10.1002/anie.202204144
    Scopus Count
    Collections
    Articles; Physical Science and Engineering (PSE) Division; Chemical Science Program; KAUST Catalysis Center (KCC)

    entitlement

     
    DSpace software copyright © 2002-2022  DuraSpace
    Quick Guide | Contact Us | KAUST University Library
    Open Repository is a service hosted by 
    Atmire NV
     

    Export search results

    The export option will allow you to export the current search results of the entered query to a file. Different formats are available for download. To export the items, click on the button corresponding with the preferred download format.

    By default, clicking on the export buttons will result in a download of the allowed maximum amount of items. For anonymous users the allowed maximum amount is 50 search results.

    To select a subset of the search results, click "Selective Export" button and make a selection of the items you want to export. The amount of items that can be exported at once is similarly restricted as the full export.

    After making a selection, click one of the export format buttons. The amount of items that will be exported is indicated in the bubble next to export format.