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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ArticleAuthors
Ghosh, ArnabMane, Manoj Vasisht

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
2020-02-24Online Publication Date
2020-02-24Print Publication Date
2020-03-16Submitted Date
2019-12-16Permanent link to this record
http://hdl.handle.net/10754/661552
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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.201901754Sponsors
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
WileyJournal
Chemistry – An Asian JournalAdditional Links
https://onlinelibrary.wiley.com/doi/abs/10.1002/asia.201901754ae974a485f413a2113503eed53cd6c53
10.1002/asia.201901754