Journal article
Asymmetric synthesis of α-hydroxy carboxylic acids: direct oxidation of chiral amide enolates using 2-sulfonyloxaziridines
Tetrahedron letters, v 26(30), pp 3539-3542
1985
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
The direct oxidation of chiral amide enolates to optically active mandelic acid using 2-sulfonyloxaziridine
1
is described. The diastereoselectivity is counterion dependent.
Metrics
Details
- Title
- Asymmetric synthesis of α-hydroxy carboxylic acids: direct oxidation of chiral amide enolates using 2-sulfonyloxaziridines
- Creators
- Franklin A. Davis - Drexel UniversityLal C. Vishwakarma - Drexel University
- Publication Details
- Tetrahedron letters, v 26(30), pp 3539-3542
- Publisher
- Elsevier
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Neurobiology and Anatomy; [Retired Faculty]
- Web of Science ID
- WOS:A1985AMQ3400006
- Scopus ID
- 2-s2.0-0001237102
- Other Identifier
- 991019174149204721
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InCites Highlights
Data related to this publication, from InCites Benchmarking & Analytics tool:
- Web of Science research areas
- Chemistry, Organic