Journal article
Asymmetric epoxidation of nonfunctionalized alkenes with high enantioselectivity using chiral sulfamyloxaziridines
Tetrahedron letters, v 27(42), pp 5079-5082
1986
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
High enantioselectivities (19–65% ee) are reported for the asymmetric epoxidation of a series of nonfunctionalized alkenes using chiral sulfamyloxaziridines (
1b
/
2b
).
The asymmetric epoxidatlon of nonfunctionalized alkenes (19–65% ee) using chiral 2-sulfamyloxaziridines is described.
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Details
- Title
- Asymmetric epoxidation of nonfunctionalized alkenes with high enantioselectivity using chiral sulfamyloxaziridines
- Creators
- Franklin A. Davis - Drexel UniversitySankar Chattopadhyay - Drexel University
- Publication Details
- Tetrahedron letters, v 27(42), pp 5079-5082
- Publisher
- Elsevier
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:A1986E469400009
- Scopus ID
- 2-s2.0-0001400976
- Other Identifier
- 991019173664704721
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InCites Highlights
Data related to this publication, from InCites Benchmarking & Analytics tool:
- Web of Science research areas
- Chemistry, Organic