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.
Diasteoselective conjugate additions reactions of a lithiated allylic sulfoximine to acyclic enones
Journal ArticleOverview
UOW Authors
Publication Date
- 1994
Publisher
Published In
Background
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
Identity
Digital Object Identifier (doi)
Scopus Eid
- 2-s2.0-37049089774
Web Of Science Accession Number
Additional Document Info
Start Page
- 751
End Page
- 752
Issue
- 6
Overview
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.
UOW Authors
Publication Date
- 1994
Publisher
Published In
Background
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
Identity
Digital Object Identifier (doi)
Scopus Eid
- 2-s2.0-37049089774
Web Of Science Accession Number
Additional Document Info
Start Page
- 751
End Page
- 752
Issue
- 6