Issue 23, 1986

Asymmetric intramolecular conjugate addition of amines to chiral vinyl sulphoxides. Total synthesis of (R)-(+)-carnegine

Abstract

The (E)- and (Z)-vinyl sulphoxides (3) and (4) upon treatment with base, undergo cyclization to give chiral isoquinolines one of which was converted into (R)-(+)-carnegine.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 1688-1689

Asymmetric intramolecular conjugate addition of amines to chiral vinyl sulphoxides. Total synthesis of (R)-(+)-carnegine

S. G. Pyne and S. L. Chapman, J. Chem. Soc., Chem. Commun., 1986, 1688 DOI: 10.1039/C39860001688

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