Issue 22, 1989

Palladium-catalysed intramolecular asymmetric ene reaction of chiral allylic sulphones via chiral allylic sulphinate–sulphone rearrangements

Abstract

The chirality of the sulphinate sulphur atoms has been transferred to the carbon centres in chiral allylic sulphinate–sulphone rearrangements, followed by palladium-catalysed intramolecular ene reactions of the chiral allylic sulphones obtained, with high stereospecificity.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1778-1780

Palladium-catalysed intramolecular asymmetric ene reaction of chiral allylic sulphones via chiral allylic sulphinate–sulphone rearrangements

K. Hiroi and Y. Kurihara, J. Chem. Soc., Chem. Commun., 1989, 1778 DOI: 10.1039/C39890001778

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