Preparation of 1-(9-anthryl)-ethanol and 9-anthryloxirane via catalytic enantioselective reduction of prochiral 9-anthryl ketones
โ Scribed by I. Reiners; J. Martens
- Book ID
- 104360934
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 120 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0957-4166
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โฆ Synopsis
Enantioselective reduction of prochiral 9-anthryl ketones to the corresponding chiral alcohols proceeds with high enantiomeric excess. The chiral alcohol 1-(9-anthryl)-2-bromo-ethanol can be converted to the corresponding chiral oxirane. (~
๐ SIMILAR VOLUMES
New Chiral Borohydride Based Reducing Agent: Asymmetric Reduction of 9-Anthryl Trifluoromethyl Ketone and Other Carbonyl Compounds. -The first report of two chiral borohydride agents, prepared from 1,2-aminoalcohols and NaBH 4 , and their use in the reduction of ketones (I) to the corresponding chir
Aqueous micellar solutions containing cetyltrimethylammonium bromide (CTAB) and solubilized 2,2,2-trifluoro-1-( 9 -anthryl)-ethanol (TFAE) known to exhibit photorheological effects were investigated via (i) oscillatory shear viscometry, (ii) electrically induced birefringence, and (iii) dynamic ligh