Journal article
Oxidation of enamines to α-hydroxy ketones and α-amino ketones using N-sulfonyloxaziridines
Tetrahedron letters, v 29(35), pp 4365-4368
1988
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Tri-substituted enamines are oxidized to α-hydroxy ketones by N-sulfonyloxaziridines while di-substituted enamines are oxidized to α-amino ketones. A unified mechanism for the formation of both α-hydroxy ketones and α-amino ketones is proposed.
Tri-substituted enamines are oxidized to α-hydroxy ketones by N-sulfonyloxaziridines [
O] while di-substituted enamines are oxidized to α-amino ketones. A unified mechanism for the formation of both α-hydroxy ketones and α-amino ketones is proposed.
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Details
- Title
- Oxidation of enamines to α-hydroxy ketones and α-amino ketones using N-sulfonyloxaziridines
- Creators
- Franklin A. Davis - Drexel UniversityAurelia C. Sheppard - Drexel University
- Publication Details
- Tetrahedron letters, v 29(35), pp 4365-4368
- Publisher
- Elsevier
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:A1988Q440700003
- Scopus ID
- 2-s2.0-0001033778
- Other Identifier
- 991019173867704721
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Data related to this publication, from InCites Benchmarking & Analytics tool:
- Web of Science research areas
- Chemistry, Organic