Issue 17, 1970

Participation by the nitro-group in the ring-opening reactions of substituted o-nitrophnylethylene oxides

Abstract

Ethereal hydrogen chloride converts substituted o-nitrophenylethylene oxides into products identified as tautomeric 3,4-dihydro-1,3-dihydroxy-4-oxoquinoline derivatives: a course for these reactions involving participation by the nitro-group in the acid-catalysed opening of the epoxide ring is discussed.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 1100-1102

Participation by the nitro-group in the ring-opening reactions of substituted o-nitrophnylethylene oxides

T. W. M. Spence and G. Tennant, J. Chem. Soc. D, 1970, 1100 DOI: 10.1039/C29700001100

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