Issue 0, 1971

Heterocyclic rearrangements. Part XIII. The conversion of a nitro-2,1-benzisoxazole into an acylbenzofurazan, and some unsuccessful rearrangements and oxygen transfer reactions

Abstract

3-Methyl-7-nitro-2,1-benzisoxazole is converted by trimethylphosphite into 4-acetylbenzofurazan. The preparation is described of several indazoles and benzotriazoles as possible precursors for analogous rearrangements. 1,10-Phenanthroline 1-oxide fails to undergo intramolecular oxygen transfer.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 1193-1196

Heterocyclic rearrangements. Part XIII. The conversion of a nitro-2,1-benzisoxazole into an acylbenzofurazan, and some unsuccessful rearrangements and oxygen transfer reactions

A. J. Boulton, I. J. Fletcher and A. R. Katritzky, J. Chem. Soc. C, 1971, 1193 DOI: 10.1039/J39710001193

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