Issue 24, 1986

Intramolecular cyclopropanation of an aromatic nucleus by an alkylidenecarbene: a novel access to heptafulvenes

Abstract

Thermolysis of the α-diazoketone (1) at 80 °C generates the electron-rich heptafulvene (2); the alkylidenecarbene (5) is the key intermediate of the reaction sequence.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 1782-1783

Intramolecular cyclopropanation of an aromatic nucleus by an alkylidenecarbene: a novel access to heptafulvenes

R. Brückmann and G. Maas, J. Chem. Soc., Chem. Commun., 1986, 1782 DOI: 10.1039/C39860001782

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