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

Citation

• Pyne, S. G., & Chapman, S. L. (1986). Asymmetric intramolecular conjugate addition of amines to chiral vinyl sulphoxides. Total synthesis of (R)-(+)-Carnegine. Journal of the Chemical Society - Series Chemical Communications, 1688-1689. doi:10.1039/C39860001688

Digital Object Identifier (doi)

• 10.1039/C39860001688

Scopus Eid

• 2-s2.0-37049067217

Web Of Science Accession Number

Start Page

• 1688

End Page

• 1689

Abstract

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

UOW Authors

•   Pyne, Stephen

Publication Date

• 1986

Publisher

• Royal Society of Chemistry (RSC) 

Published In

• Journal of the Chemical Society - Series Chemical Communications  Journal

Citation

• Pyne, S. G., & Chapman, S. L. (1986). Asymmetric intramolecular conjugate addition of amines to chiral vinyl sulphoxides. Total synthesis of (R)-(+)-Carnegine. Journal of the Chemical Society - Series Chemical Communications, 1688-1689. doi:10.1039/C39860001688

Digital Object Identifier (doi)

• 10.1039/C39860001688

Scopus Eid

• 2-s2.0-37049067217

Web Of Science Accession Number

Start Page

• 1688

End Page

• 1689