Issue 12, 1997

1,3-Dipolar Cycloaddition of Arylnitrile Oxides to Some Exocyclic Alkenes and Regioselective Synthesis of Spiro Isoxazolines

Abstract

The cycloaddition of arylnitrile N-oxides to the exocyclic double bond of arylmethylidenes derived from indane-1,3-dione 1a–c, indan-1-one 1d–f and 1-tetralone 1g–i afforded the spiroisoxazolines 2a–l with high regioselectivity and not the corresponding isomers 3a–l.

Article information

Article type
Paper

J. Chem. Res. (S), 1997, 438-438

1,3-Dipolar Cycloaddition of Arylnitrile Oxides to Some Exocyclic Alkenes and Regioselective Synthesis of Spiro Isoxazolines

N. Mishriky, F. M. Asaad, Y. A. Ibrahim and A. S. Girgis, J. Chem. Res. (S), 1997, 438 DOI: 10.1039/A702066J

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