Issue 3, 1986

Acid catalysis in the intramolecular addition of α-lithiosulphoxides to isolated double bonds

Abstract

Intramolecular addition of a α-sulphinyl carbanion to an isolated double bond is observed with mesocyclic metallated E homoallylic sulphoxides (1) and (2); kinetic data suggest that this process is acid catalysed and that free (1) is the proton donor species.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 223-224

Acid catalysis in the intramolecular addition of α-lithiosulphoxides to isolated double bonds

V. Cerè, C. Paolucci, S. Pollicino, E. Sandri and A. Fava, J. Chem. Soc., Chem. Commun., 1986, 223 DOI: 10.1039/C39860000223

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