Catalyst-free regioselective [3+2] cycloadditions of alpha,beta-unsaturated N-arylnitrones with alkenes to access functionalized isoxazolidines: a DFT study

TitleCatalyst-free regioselective [3+2] cycloadditions of alpha,beta-unsaturated N-arylnitrones with alkenes to access functionalized isoxazolidines: a DFT study
Publication TypeJournal Article
Year of Publication2020
AuthorsGhosh, A, Mane, MV, Rode, HB, Patil, SA, Sridhar, B, Dateer, RB
JournalChemistry-An Asian Journal
Volume15
Issue6
Pagination899-903
Date PublishedMAR
Type of ArticleArticle
ISSN1861-4728
KeywordsDFT study, isoxazolidines, metal and ligand free, nitrone cycloaddition, Regioselective
Abstract

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.

DOI10.1002/asia.201901754, Early Access Date = FEB 2020
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

4.056

Divison category: 
Physical and Materials Chemistry

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