ChemInform Abstract: Kinetic Resolution of Secondary Alcohols. Enantioselective Acylation Mediated by a Chiral (Dimethylamino)pyridine Derivative.
β Scribed by E. VEDEJS; X. CHEN
- Book ID
- 112033232
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
Nonenzymatic Enantioselective Acylation of Racemic Secondary Alcohols Catalyzed by a SnX2-Chiral Diamine Complex. -Under the optimized conditions shown a kinetic nonenzymatic resolution is achieved with different kinds of racemic secondary alcohols. -(ORIYAMA, T.; HORI,
1997 stereochemistry stereochemistry (general, optical resolution) O 0030 20 -034 Effective Kinetic Resolution of Secondary Alcohols with a Planar-Chiral Analogue of 4-(Dimethylamino)pyridine. Use of the Fe(C5Ph5) Group in Asymmetric Catalysis. -The stereoselectivity displayed by the shown catalyst
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