Enantioselective reduction of ketones with borane catalyzed by cyclic β- amino alcohols prepared from proline
✍ Scribed by Ayhan S Demir; Idris Mecitoglu; Cihangir Tanyeli; Volkan Gülbeyaz
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 359 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0957-4166
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✦ Synopsis
New catalysts have been prepared from (S)-and (R)-proline and the asymmetric borane reduction of prochiral ketones using these catalysts has been studied. The secondary alcohols were obtained in 76-95% yield with 57-96 % enantiomerie excesses.
📜 SIMILAR VOLUMES
## Abstract In the presence of tridentate chiral ligand **4e**, 99% e.e. value was obtained by asymmetric reduction of ethyl benzoylacetate with borane in toluene at 25°C. Various ligands and reaction conditions were investigated to develop a reasonable mechanism that explains the experimental outc
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v