Enantioselective catalytic borane reductions of achiral ketones: Syntheses and application of two chiral β-amino alcohols from (S)-2-indoline carboxylic acid
暂无分享,去创建一个
[1] T. Tarnai,et al. Enantioselective hydrogenation of acetophenone in the presence of S-proline , 1991 .
[2] V. Nevalainen. Quantum chemical modeling of chiral catalysis. Part 3. On the role of a Lewis basic solvent in the mechanism of catalytic enantioselective reduction of carbonyl compounds by chiral oxazaborolidines , 1991 .
[3] V. Nevalainen. Quantum chemical modeling of chiral catalysis. On the mechanism of catalytic enantioselective reduction of carbonyl compounds by chiral oxazaborolidines , 1991 .
[4] V. Nevalainen. Quantum chemical modeling of chiral catalysis. Part 2. On the origin of enantioselection in the coordination of carbonyl compounds to borane adducts of chiral oxazaborolidines , 1991 .
[5] V. Nevalainen. Quantum chemical modeling of chiral catalysis. Part 4. On the hydride transfer in ketone complexes of borane adducts of oxazaborolidines and regeneration of the catalyst , 1991 .
[6] H. Blaser. Enantioselective synthesis using chiral heterogeneous catalysts. , 1991 .
[7] John M. Brown,et al. CATALYTIC ASYMMETRIC HYDROBORATION WITH OXAZABOROLIDINES , 1991 .
[8] M. K. Gurjar,et al. Enantioselective reductions of ketones with oxazaborolidines derived from (R and (S-α-α-diphenyl-2-piperdine methanol , 1990 .
[9] C. Pak,et al. Asymmetric borane reduction of ketones catalyzed by oxazaborolidine , 1988 .
[10] E. Corey,et al. A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses , 1987 .
[11] P. Ramachandran,et al. Selective reductions. 40. A critical examination of the relative effectiveness of various reducing agents for the asymmetric reduction of different classes of ketones , 1987 .
[12] E. Corey,et al. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications , 1987 .
[13] Koichi Ito,et al. Catalytic Behavior of Optically Active Amino Alcohol–Borane Complex in the Enantioselective Reduction of Acetophenone Oxime O-Alkyl Ethers , 1987 .
[14] T. Collier,et al. Recent advances in asymmetric synthesis-II , 1986 .
[15] C. Pak,et al. Magnesium-methanol as a simple convenient reducing agent for α,β -unsaturated esters , 1986 .
[16] H. Haubenstock. Asymmetric Reductions with Chiral Complex Aluminum Hydrides and Tricoordinate Aluminum Reagents , 2007 .
[17] H. Mosher,et al. Asymmetric reductions with chiral reagents from lithium aluminum hydride and (+)-(2S,3R)-4-dimethylamino-3-methyl-1,2-diphenyl-2-butanol , 1973 .
[18] E. Corey,et al. Studies on the symmetric synthesis of alpha-amino acids. II. New systems for highly specific asymmetric synthesis with conservation of the Chiral reagent. , 1970, Journal of the American Chemical Society.
[19] E. Corey,et al. Studies on the asymmetric synthesis of alpha-amino acids. I. A new approach. , 1970, Journal of the American Chemical Society.
[20] A. G. Davies,et al. 633. The resolution and reactions of 1 : 2 : 3 : 4-tetrahydro-1-naphthol. A new preparation of 1 : 2 : 3 : 4-tetrahydro-1-naphthyl hydroperoxide , 1952 .
[21] T. Collyer,et al. 126. The resolution of β-naphthylmethylcarbinol , 1940 .
[22] J. Kenyon,et al. CVII.—Investigations on the dependence of rotatory power on chemical constitution. Part VI. The optical rotatory power of methyl-tert.-butyl-, methylbenzyl-, methylphenylethyl- and methyl-α-naphthyl-carbinols , 1914 .