Journal article
Diastereoselective fluorination of chiral imide enolates using n-fluoro- o-benzenedisulfonimide (nfobs)
Tetrahedron letters, v 33(9), pp 1153-1156
1992
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
α-Fluoro acids (78–90% ee) and β-fluoro alcohols (89–>95%ee) of well defined stereochemistry are prepared via the diastereoselective fluorination of chiral imide enolates with NFOBS (3).
α-Fluoro acids and β-fluoro alcohols of well defined stereochemistry are prepared via the diastereoselective fluorination of chiral imide enolates with N-fluoro-
o-benzenedisulfonimide (NFOBS).
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Details
- Title
- Diastereoselective fluorination of chiral imide enolates using n-fluoro- o-benzenedisulfonimide (nfobs)
- Creators
- Franklin A. Davis - Drexel UniversityWei Han - Drexel University
- Publication Details
- Tetrahedron letters, v 33(9), pp 1153-1156
- Publisher
- Elsevier
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- [Retired Faculty]
- Web of Science ID
- WOS:A1992HF62600007
- Scopus ID
- 2-s2.0-0026500332
- Other Identifier
- 991019173724004721
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Data related to this publication, from InCites Benchmarking & Analytics tool:
- Web of Science research areas
- Chemistry, Organic