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   <subfield code="a">Synthesis of some novel fluoro isoxazolidine and isoxazoline derivatives using N -benzyl fluoro nitrone via cycloaddition reaction in ionic liquid</subfield>
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   <subfield code="a">1-Butyl-3-methylimidazolium-based ionic liquids are found to accelerate significantly the intermolecular 1,3-dipolar cycloaddition of N-benzyl-fluoro nitrone derived in situ from 2,6-difluoro benzaldehyde and N-benzylhydroxylamine, with activated alkenes and electron deficient alkynes to afford enhanced rates and improved yields of novel isoxazolidines and isoxazolines. Graphical Abstract 1-Butyl-3-methylimidazolium-based ionic liquids are found to accelerate significantly the intermolecular 1,3-dipolar cycloaddition of N-benzyl-fluoro nitrone derived in situ from 2,6-difluoro benzaldehyde and N-benzylhydroxylamine, with activated alkenes and electron deficient alkynes to afford enhanced rates and improved yields of novel isoxazolidine, isoxazolines.</subfield>
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