14 results on '"Ema, Tadashi"'
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2. Reestimation of the Taft's substituent constant of the pentafluorophenyl group
3. 5-[4-(1-hydroxyethyl)phenyl]-10,15,20-triphenylporphyrin as a probe of the transition-state conformation in hydrolase-catalyzed enantioselective transesterifications
4. Lipase-catalyzed transesterification of 2-hydroxy-2-(pentafluorophenyl)acetonitrile leading to (1R,2R)-and (1S,2S)-bis(pentafluorophenyl)ethane-1,2-diol
5. Highly enantioselective reduction of carbonyl compounds using a reductase purified from bakers' yeast
6. Kinetic resolution of racemic 2-substituted 3-cyclopenten-1-ols by lipase-catalyzed transesterifications: a rational strategy to improve enantioselectivity
7. High enantioselectivity and broad substrate specificity of a carbonyl reductase: toward a versatile biocatalyst
8. Synthesis and evaluation of chiral selectors with multiple hydrogen-bonding sites in the macrocyclic cavities
9. Tuning the chiral cavity of macrocyclic receptor for chiral recognition and discrimination
10. Lipase-catalyzed resolution of [2R(super *),3S(super *)]-and [2R(super *),3R(super *)]-3-methyl-3-phenyl-2-aziridinemethanol at low temperatures and determination of the absolute configurations of the four stereoisomers
11. Cross-Coupling Approach to an Array of Macrocyclic Receptors Functioning as Chiral Solvating Agents.
12. Enhancement of the enantioselectivity in lipase-catalyzed kinetic resolutions of 3-phenyl-2H-azirine-2-methanol by lowering the temperature to -40 degrees Celsius
13. Lipase-Catalyzed Resolution of (2R*,3S*)- and (2R*,3R*)-3-Methyl-3-phenyl-2-aziridinemethanol at Low Temperatures and Determination of the Absolute Configurations of the Four Stereoisomers.
14. Synthesis of Enamines, Aldehydes, and Nitriles from CO 2 : Scope of the One-Pot Strategy via Formamides.
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