Abstract
By appropriate choice of reaction conditions, the same enantiomerically pure (S)-(+)-2-(p-tolylsulfinyl)cycloalkenone can be converted into either an (R)-or an (S)-3-substituted cycloalkanone in good to excellent enantiomeric purity.
- Title
- Enantiocontrolled synthesis of (S)-3-substituted cycloalkanones from (s)-2-(p-tolylsulfinyl)-2-cycloalkenones and diorganomagnesium reagents.
- Creators
- Gary H. Posner (Author) - Johns Hopkins UniversityMartin Hulce (Author) - Johns Hopkins University
- Additional links
- Anon
- Publication Details
- Tetrahedron Letters, Vol.25(4), pp.379-382
- Series
- 25
- Number of pages
- 4
- Identifiers
- 991005930564202656
- Academic Unit
- Creighton University
- Language
- English
- Resource Type
- Journal article