Journal article
Influence of enolate geometry and structure on the stereochemistry of the asymmetric oxidation of prochiral ketone enolates to optically active α-hydroxy ketones
Tetrahedron letters, v 30(7), pp 779-782
1989
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
The stereoselectivity for the asymmetric oxidation of enolates to optically active α-hydroxy ketones using (+)-(camphorylsulfonyl)oxaziridine is dependent on the enolate substitution pattern, the solution structure of the enolate and to a lesser extent the enolate geometry.
The stereoselectivity for the asymmetrix oxidation of enolates to optically active α-hydroxy ketones using (+)-(camphoryl-sulfonyl)oxaziridine is dependent on the enolate substitution pattern, the solution structure of the enolate and to a lesser extent the enolate geometry.
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Details
- Title
- Influence of enolate geometry and structure on the stereochemistry of the asymmetric oxidation of prochiral ketone enolates to optically active α-hydroxy ketones
- Creators
- Franklin A. Davis - Drexel UniversityAurelia C. Sheppard - Drexel UniversityG.Sankar Lal - Drexel University
- Publication Details
- Tetrahedron letters, v 30(7), pp 779-782
- Publisher
- Elsevier
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:A1989T425500001
- Scopus ID
- 2-s2.0-33748178028
- Other Identifier
- 991019174732804721
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InCites Highlights
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- Web of Science research areas
- Chemistry, Organic