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    Catalyst-Free Regioselective (3+2)-Cycloadditions of α, β-unsaturated N -arylnitrones with Alkenes to Access Functionalized Isoxazolidines: A DFT Study.

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    _Ghosh_et_al-2020-Chemistry_-_An_Asian_Journal.pdf
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    Type
    Article
    Authors
    Ghosh, Arnab
    Mane, Manoj Vasisht cc
    Rode, Haridas
    Patil, Siddappa
    Sridhar, Balasubramanian
    Dateer, Ramesh
    KAUST Department
    KAUST Catalysis Center (KCC)
    King abdullah university of science and technology, KAUST catalysis centre, SAUDI ARABIA.
    Physical Science and Engineering (PSE) Division
    Date
    2020-02-24
    Online Publication Date
    2020-02-24
    Print Publication Date
    2020-03-16
    Submitted Date
    2019-12-16
    Permanent link to this record
    http://hdl.handle.net/10754/661552
    
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    Abstract
    The catalyst-free regioselective [3+2]-cycloaddition of α, β-unsaturated N -arylnitrones with alkenes are developed. The series of synthetically important functionalized isoxazolidines are prepared in good to excellent yields by step economic pathway under ligand and transition metal-free condition. The regioselective cycloaddition pathway supported by control experiment and computational study.
    Citation
    Ghosh, A., Mane, M., Rode, H., Patil, S., Sridhar, B., & Dateer, R. (2020). Catalyst-Free Regioselective (3+2)-Cycloadditions of α, β-unsaturated N -arylnitrones with Alkenes to Access Functionalized Isoxazolidines: A DFT Study. Chemistry – An Asian Journal. doi:10.1002/asia.201901754
    Sponsors
    he authors thank, DST-SERB, Government of India, for the financial support through the research grant: FileNos. SB/S2/RJN-042/2017 andECR/2017/002207.Author also thanks to Jain University, India, for financial support.
    Publisher
    Wiley
    Journal
    Chemistry – An Asian Journal
    DOI
    10.1002/asia.201901754
    Additional Links
    https://onlinelibrary.wiley.com/doi/abs/10.1002/asia.201901754
    ae974a485f413a2113503eed53cd6c53
    10.1002/asia.201901754
    Scopus Count
    Collections
    Articles; Physical Science and Engineering (PSE) Division; KAUST Catalysis Center (KCC)

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