𝔖 Bobbio Scriptorium
✦   LIBER   ✦

(S)-2-Amino-3-(2,5-dimethylphenyl)-1,1-diphenyl-1-propanol: Synthesis and Application in Enantioselective Reduction of Prochiral Ketones

✍ 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

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Enantioselective reduction of prochiral
✍ Xingshu Li; Rugang Xie πŸ“‚ Article πŸ“… 1997 πŸ› Elsevier Science 🌐 English βš– 175 KB

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

ChemInform Abstract: cis-1-Amino-1,2,3,4
✍ S. HIGASHIJIMA; H. ITOH; Y. SENDA; S. NAKANO πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 28 KB πŸ‘ 1 views

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