Synthesis of novel isoxazolidines via 1,3-dipolar cycloaddition of nitrones to olefins

DOI: 10.1515/HC.2003.9.2.161

Source and publish data:

Heterocyclic Communications p. 161 - 164 (2003)

Update date:2022-08-03

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Authors:

Vishu Kumar

Mantelingu

Basappa Basappa

Rangappa

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Article abstract of DOI:10.1515/HC.2003.9.2.161

C-anthranyl-N-3-methylphenyl nitrone has been discovered as new 1,3-dipole to form N-arylisoxazolidines via 1,3-dipolar cycloaddition reaction with olefins. Synthesized novel isoxazolidines were characterized by ¹H NMR, IR and C, H and N analys

Full text of DOI:10.1515/HC.2003.9.2.161

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Article Doi

Synthesis of novel isoxazolidines via 1,3-dipolar cycloaddition of nitrones to olefins

DOI: 10.1515/HC.2003.9.2.161

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Article abstract of DOI:10.1515/HC.2003.9.2.161

Full text of DOI:10.1515/HC.2003.9.2.161

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