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

Arnab Ghosh, Manoj Mane, Haridas Rode, Siddappa Patil, Balasubramanian Sridhar, Ramesh Dateer

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

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.
Original languageEnglish (US)
JournalChemistry, an Asian journal
DOIs
StatePublished - Feb 15 2020

Fingerprint

Dive into the research topics of 'Catalyst-Free Regioselective (3+2)-Cycloadditions of α, β-unsaturated N -arylnitrones with Alkenes to Access Functionalized Isoxazolidines: A DFT Study.'. Together they form a unique fingerprint.

Cite this