Issue 0, 1979

Acid-promoted behaviour of 1a,7b-dihydro-1H-cyclopropa[c]cinnolines

Abstract

Compounds (1 a–c) undergo in boiling acetic acid a fast reaction to afford 1,4-dihydrocinnolines or 4,5-dihydro1H-1,2-benzodiazepines, which arise from a skeleton rearrangement involving cleavage of the cyclopropane ring. Fragmentation products are also obtained in the case of (1c).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1979, 1195-1198

Acid-promoted behaviour of 1a,7b-dihydro-1H-cyclopropa[c]cinnolines

L. Garanti and G. Zecchi, J. Chem. Soc., Perkin Trans. 1, 1979, 1195 DOI: 10.1039/P19790001195

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