Kinetic Study of the Hydrolysis of Schiff Bases Derived from 2-Aminothiophenol

Author:

Hassib Hekmat B.,Abdel-Kader Nora S.,Issa Yousry M.

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry,Molecular Biology,Biochemistry,Biophysics

Reference16 articles.

1. Belokon, Y.N., Kochetkov, K.A., Plieva, F.M., Ikonnikov, N.S., Maleev, V.I., Parmar, V.S., Kumar, R., Lozinsky, V.I.: Enantioselective hydrolysis of a Schiff’s base of d, l-phenylalanine ethyl ester in water-poor media via the reaction catalyzed with α-chymotrypsin immobilized on hydrophilic macroporous gel support. Appl. Biochem. Biotechnol. 84, 97–106 (2000)

2. Parmar, V.S., Singh, A., Bisht, K.S., Kumar, N., Belokon, Y.N., Kochetkov, K.A., Ikonnikov, N.S., Orlova, S.A., Tararov, V.I., Saveleva, T.F.: Schiff bases of amino acid esters as new substrates for the enantioselective enzymatic hydrolysis and accompanied asymmetric transformations in aqueous organic solvents. J. Org. Chem. 61, 1223–1227 (1996)

3. Garcia Del Vado, M.A., Rodriguez Cardona, F., Echevarria, G., Martinez Gonzalez, C., Santos Blanco, J.G., Garcia Blanco, F.: Determination of the rates of formation and hydrolysis of the Schiff bases formed by pyridoxal and poly-l-lysine. J. Mol. Catal. 87, 361–370 (1994)

4. Jiang, W., Xu, B., Zhong, J., Li, J., Liu, F.: Hydrolytic cleavage of bis(p-nitrophenyl) phosphate by Schiff base MnIII complexes containing morpholine pendants in Gemini 16–6-16 micelles. J. Chem. Sci. 120, 411–417 (2008)

5. Gorostidi, G.R.E., Santos, J.G., Basagoitia, A., Blanco, F.G.: Determination of the rates of formation and hydrolysis of the Schiff bases formed by pyridoxal 5′-phosphate with l-tryptophan and its methyl and n-butyl esters. Bull. Chem. Soc. Japan 75, 2471–2476 (2002)

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