(S)-2-Amino-3-(2,5-dimethylphenyl)-1,1-diphenyl-1-propanol: Synthesis and Application in Enantioselective Reduction of Prochiral Ketones
β Scribed by Zhang, Ya-Wen; Shen, Zong-Xuan; Gu, De-Ben; Chen, Wei-Yi; Fei, Zheng-Hao; Dai, Qing-Fei
- Book ID
- 111641901
- Publisher
- Taylor and Francis Group
- Year
- 1996
- Tongue
- English
- Weight
- 203 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0039-7911
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π SIMILAR VOLUMES
Two new optically active l~-amino alcohols 1 and 2 were prepared from Lcystine. The in situ formed chiral oxazaborolidines have been used in the enantioselective catalytic homogeneous borane reduction of prochiral ketones and diketones. The chiral secondary alcohols are obtained with moderate to goo
cis-1-Amino-1,2,3,4-tetrahydro-2-naphthalenol: Resolution and Application to the Catalytic Enantioselective Reduction of Ketones. -The optically active title amino alcohols are prepared by optical resolution of racemic amino alcohols with (-)-mandelic acid and used in the asymmetric reduction of ke