@article {46952,
	title = {Catalyst-free regioselective [3+2] cycloadditions of alpha,beta-unsaturated N-arylnitrones with alkenes to access functionalized isoxazolidines: a DFT study},
	journal = {Chemistry-An Asian Journal},
	volume = {15},
	year = {2020},
	month = {MAR},
	pages = {899-903},
	type = {Article},
	abstract = {<p>The catalyst-free regioselective [3+2]-cycloaddition of alpha,beta-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 conditions. The regioselective cycloaddition pathway supported by control experiment and computational study.</p>
},
	keywords = {DFT study, isoxazolidines, metal and ligand free, nitrone cycloaddition, Regioselective},
	issn = {1861-4728},
	doi = {10.1002/asia.201901754, Early Access Date = FEB 2020},
	author = {Ghosh, Arnab and Mane, Manoj V. and Rode, Haridas B. and Patil, Siddappa A. and Sridhar, Balasubramanian and Dateer, Ramesh B.}
}
