Asymmetric Intramolecular Conjugate Addition of Amines to Chiral Vinyl Sulphoximides. Total Synthesis of (R)-(+)- and (S)-(-)-Carnegine

DOI: 10.1039/c39860001686

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Journal of the Chemical Society. Chemical communications p. 1686 - 1687 (1986)

Update date:2022-08-03

Topics:: Authors:

Pyne, Stephen G.

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Article abstract of DOI:10.1039/c39860001686

The chiral vinyl sulphoximides (3a) and (3b) upon treatment with base, undergo cyclization to give chiral isoquinolines which were converted into (R)-(+)- and (S)-(-)-carnegine.

Full text of DOI:10.1039/c39860001686

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Asymmetric Intramolecular Conjugate Addition of Amines to Chiral Vinyl Sulphoximides. Total Synthesis of (R)-(+)- and (S)-(-)-Carnegine

DOI: 10.1039/c39860001686

Source and publish data:

Authors:

Article abstract of DOI:10.1039/c39860001686

Full text of DOI:10.1039/c39860001686

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