Journals / Turkish Journal of Chemistry / 2005 / Cilt: 29 - Sayı: 2

Synthesis of Some New Isoxazolidines by 1,3-Dipolar Cycloaddition Reaction of Nitrones and Olefins

Pages
147–152
DOI
—

Abstract

A series of new isoxazolidines 5a-j were synthesized by 1,3-dipolar cycloaddition reaction of different nitrones with substituted olefins under reflux condition. The yields of products following recrystallization from absolute ethanol were of the order of 40%-66%. IR, NMR and mass spectroscopies were used for identification of these compounds.

Özet

A series of new isoxazolidines 5a-j were synthesized by 1,3-dipolar cycloaddition reaction of different nitrones with substituted olefins under reflux condition. The yields of products following recrystallization from absolute ethanol were of the order of 40%-66%. IR, NMR and mass spectroscopies were used for identification of these compounds.

Keywords: Isoxazolidine, Nitrones, 1, 3-Dipolar, Cycloaddition