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Diastereoselective reactions of allylic sulfoximine anions

Journal Article


Abstract


  • The conjugate addition reactions of lithiated N-p-tolyl S-phenyl S-2-propenyl sulfoximine (4) with cyclic and acyclic enones gives exclusively 1,4-a adducts, the reactions with acyclic enones are highly diastereoselective. © 1994, Taylor & Francis Group, LLC. All rights reserved.

Publication Date


  • 1994

Citation


  • Pyne, S. G., & Dong, Z. (1994). Diastereoselective reactions of allylic sulfoximine anions. Phosphorus, Sulfur, and Silicon and the Related Elements, 95(1-4), 425-426. doi:10.1080/10426509408034262

Scopus Eid


  • 2-s2.0-36349010395

Web Of Science Accession Number


Start Page


  • 425

End Page


  • 426

Volume


  • 95

Issue


  • 1-4

Abstract


  • The conjugate addition reactions of lithiated N-p-tolyl S-phenyl S-2-propenyl sulfoximine (4) with cyclic and acyclic enones gives exclusively 1,4-a adducts, the reactions with acyclic enones are highly diastereoselective. © 1994, Taylor & Francis Group, LLC. All rights reserved.

Publication Date


  • 1994

Citation


  • Pyne, S. G., & Dong, Z. (1994). Diastereoselective reactions of allylic sulfoximine anions. Phosphorus, Sulfur, and Silicon and the Related Elements, 95(1-4), 425-426. doi:10.1080/10426509408034262

Scopus Eid


  • 2-s2.0-36349010395

Web Of Science Accession Number


Start Page


  • 425

End Page


  • 426

Volume


  • 95

Issue


  • 1-4