TY - JOUR
T1 - Catalyst-Free Regioselective (3+2)-Cycloadditions of α, β-unsaturated N -arylnitrones with Alkenes to Access Functionalized Isoxazolidines: A DFT Study.
AU - Ghosh, Arnab
AU - Mane, Manoj
AU - Rode, Haridas
AU - Patil, Siddappa
AU - Sridhar, Balasubramanian
AU - Dateer, Ramesh
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: 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.
PY - 2020/2/15
Y1 - 2020/2/15
N2 - 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.
AB - 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.
UR - http://hdl.handle.net/10754/661552
UR - https://onlinelibrary.wiley.com/doi/abs/10.1002/asia.201901754
U2 - 10.1002/asia.201901754
DO - 10.1002/asia.201901754
M3 - Article
C2 - 32056350
SN - 1861-4728
JO - Chemistry, an Asian journal
JF - Chemistry, an Asian journal
ER -