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Diasteoselective conjugate additions reactions of a lithiated allylic sulfoximine to acyclic enones

Journal Article


Abstract


  • The conjugate addition reactions of lithiated N-p-tosyl S-phenyl-2-enyl sulfoximine 4 with cyclic and acyclic enones gives exclusively 1,4-α adducts, the reactions with acyclic enones are highly diastereoselective.

Publication Date


  • 1994

Citation


  • Pyne, S. G., Dong, Z., Skelton, B. W., & White, A. H. (1994). Diasteoselective conjugate additions reactions of a lithiated allylic sulfoximine to acyclic enones. Journal of the Chemical Society, Chemical Communications, (6), 751-752. doi:10.1039/C39940000751

Scopus Eid


  • 2-s2.0-37049089774

Web Of Science Accession Number


Start Page


  • 751

End Page


  • 752

Issue


  • 6

Abstract


  • The conjugate addition reactions of lithiated N-p-tosyl S-phenyl-2-enyl sulfoximine 4 with cyclic and acyclic enones gives exclusively 1,4-α adducts, the reactions with acyclic enones are highly diastereoselective.

Publication Date


  • 1994

Citation


  • Pyne, S. G., Dong, Z., Skelton, B. W., & White, A. H. (1994). Diasteoselective conjugate additions reactions of a lithiated allylic sulfoximine to acyclic enones. Journal of the Chemical Society, Chemical Communications, (6), 751-752. doi:10.1039/C39940000751

Scopus Eid


  • 2-s2.0-37049089774

Web Of Science Accession Number


Start Page


  • 751

End Page


  • 752

Issue


  • 6