Structural and optical selectivity of hydroxy ester hydrolysis by α-chymotrypsin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Acyl-Enzyme Intermediates in the α-Chymotrypsin-Catalyzed Hydrolysis of “Specific” Substrates. the Relative Rates of Hydrolysis of Ethyl, Methyl and p-Nitrophenyl Esters of N-Acetyl-L-Tryptophan
2. Hydrolysis of D-(--)-Ethyl α-Benzoyloxypropionate and L-(--)-Ethyl α-Acetoxy-β-phenylpropionate by α-Chymotrypsin
3. On the Active Site of α-Chymotrypsin
4. CCCLXXXVII.—The relationship between the optical rotatory powers and the relative configurations of optically active compounds. Part II. The relative configurations of the optically active mandelic acids and β-phenyl-lactic acids
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Resolution of Enantiomers via Biocatalysis;Topics in Stereochemistry;2007-02-26
2. Substrate modification to increase the enantioselectivity of hydrolases. A route to optically-active cyclic allylic alcohols.;Tetrahedron: Asymmetry;1993-05
3. A Summary of Ways to Obtain Optically Active Compounds;Asymmetric Synthesis;1983
4. ChemInform Abstract: STRUCTURAL AND OPTICAL SELECTIVITY OF HYDROXY ESTER HYDROLYSIS BY ALPHA-CHYMOTRYPSIN;Chemischer Informationsdienst;1975-05-06
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