Journal article
The mechanism of hydroxylation of organometallic reagents by 2-sulfonyloxaziridines
Tetrahedron letters, v 28(43), pp 5115-5118
1987
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
The hydroxylation of organometallic reagents (RM) by 2-sulfonyloxaziridines 1 is shown to involve a hemiaminal intermediate 2, whose stability is apparently related to the nucleophilicity of the hydroxylated product (ROH).
The hydroxylation of organometallic reagents (RM) by 2-sulfonyloxazirindines 1 is shown to involve a hemiaminal intermediate 2, whose stability is related to the nucleophilicity of the hydroxylated product (ROH).
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Details
- Title
- The mechanism of hydroxylation of organometallic reagents by 2-sulfonyloxaziridines
- Creators
- Franklin A. Davis - Drexel UniversityJia Wei - Drexel UniversityAurelia C. Sheppard - Drexel UniversitySteven Gubernick - Drexel University
- Publication Details
- Tetrahedron letters, v 28(43), pp 5115-5118
- Publisher
- Elsevier
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:A1987K645900017
- Scopus ID
- 2-s2.0-0000137086
- Other Identifier
- 991019173742504721
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InCites Highlights
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- Web of Science research areas
- Chemistry, Organic