Journal article
ADDITION OF DIMETHYLOXOSULFONIUM METHYLIDE TO ENANTIOMERICALLY PURE SULFINIMINES - ASYMMETRIC-SYNTHESIS OF 2-SUBSTITUTED AZIRIDINES
Tetrahedron: asymmetry, v 6(7), pp 1511-1514
01 Jul 1995
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Diastereoselective addition of dimethyloxosulfonium methylide to chiral nonracemic pure sulfinimines 1 affords N-sulfinyl aziridines 3 in 58-70% de which are readily separated. The N-sulfinyl auxiliary in 3 was removed, without ring-opening, by treatment with MeLi.
Metrics
Details
- Title
- ADDITION OF DIMETHYLOXOSULFONIUM METHYLIDE TO ENANTIOMERICALLY PURE SULFINIMINES - ASYMMETRIC-SYNTHESIS OF 2-SUBSTITUTED AZIRIDINES
- Creators
- F A Davis - Drexel UniversityP Zhou - Drexel UniversityC H Liang - Drexel UniversityR E Reddy - Drexel University
- Publication Details
- Tetrahedron: asymmetry, v 6(7), pp 1511-1514
- Publisher
- Elsevier
- Number of pages
- 4
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:A1995RR34900011
- Scopus ID
- 2-s2.0-0029144508
- Other Identifier
- 991019173838604721
UN Sustainable Development Goals (SDGs)
This publication has contributed to the advancement of the following goals:
InCites Highlights
Data related to this publication, from InCites Benchmarking & Analytics tool:
- Web of Science research areas
- Chemistry, Inorganic & Nuclear
- Chemistry, Organic
- Chemistry, Physical