Oxazolones as substrates in active site titrations of hydrolases
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference28 articles.
1. The Spectrophotometric Determination of the Operational Normality of an α-Chymotrypsin Solution
2. Electronic spectra of the isomeric 4-benzylidene-2-phenyl-Δ2-oxazolin-5-ones and the products of their reaction with nucleophiles including α-chymotrypsin
3. On the mechanism of the α-chymotrypsin-catalysed hydrolysis of 4-cis-benzylidene-2-phenyloxazolin-5-one: Evidence for covalent non-productive binding
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1. Asymmetric Addition and Cycloaddition Reactions with Ylidene‐Five‐Membered Heterocycles;Advanced Synthesis & Catalysis;2021-10-26
2. Regio- and stereoselective 1,3-dipolar cycloaddition reactions of C-aryl (or hetaryl)-N-phenylnitrones to monosubstituted ylidene malononitriles and 4-benzylidene-2-phenyloxazol-5(4H)-one;Zeitschrift für Naturforschung B;2017-04-28
3. Triphenylphosphine (PPh3) Catalyzed Erlenmeyer Reaction for Azlactones under Solvent-free Conditions;Journal of Heterocyclic Chemistry;2016-03-15
4. [Et3NH][HSO4]-mediated functionalization of hippuric acid: an unprecedented approach to 4-arylidene-2-phenyl-5(4H)-oxazolones;RSC Advances;2015
5. Synthesis, bioassay, crystal structure and ab initio studies of Erlenmeyer azlactones;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2013-03
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