Issue 14, 1977

Formation and possible intermediacy of a spiro-lactone in the nitrative cyclisation of methyl β-arylisovalerate to a nitrohydrocoumarin

Abstract

Nitration of methyl β-arylisovalerate produces a nitro spiro-lactone in addition to a nitrohydrocoumarin, suggesting possible intervention of an addition-elimination sequence in the formation of the latter compound.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 479-480

Formation and possible intermediacy of a spiro-lactone in the nitrative cyclisation of methyl β-arylisovalerate to a nitrohydrocoumarin

M. Shinoda and H. Suzuki, J. Chem. Soc., Chem. Commun., 1977, 479 DOI: 10.1039/C39770000479

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