Journal article
Stereo- and regioselective formation of silyl enol ethers via oxidation of vinyl anions
Tetrahedron letters, v 29(34), pp 4269-4272
1988
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Oxidation of E- and Z-vinyl lithiums with silyl peroxides
5 affords silyl enol ethers
3 in good to excellent yield with retention of configuration. This methodology represents a useful new procedure for the stereo- and regioselective synthesis of ketone enolates.
Oxidation of E- and Z-vinyl lithium
2 with silyl peroxides affords silyl enol ethers
3 in good to excellent yield with retention of configuration. This methodology represents a useful new procedure for the stereo- and gegioselective synthesis of ketone enolates.
Metrics
Details
- Title
- Stereo- and regioselective formation of silyl enol ethers via oxidation of vinyl anions
- Creators
- Franklin A. Davis - Drexel UniversityG. Sankar LalJia Wei - Drexel University
- Publication Details
- Tetrahedron letters, v 29(34), pp 4269-4272
- Publisher
- Elsevier
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:A1988P818800016
- Scopus ID
- 2-s2.0-45549115041
- Other Identifier
- 991019173815504721
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InCites Highlights
Data related to this publication, from InCites Benchmarking & Analytics tool:
- Web of Science research areas
- Chemistry, Organic