Phenylcarbamic acid derivatives with integrated n-phenylpiperazine moiety in the structure – kinetics of alkaline hydrolysis study / Deriváty kyseliny fenylkarbámovej s integrovanou n-fenylpiperazínovou zložkou v štruktúre – štúdium kinetiky alkalickej hydrolýzy

[1] Dittert, L. W., & Higuchi, T. Rates of hydrolysis of carbamate and carbonate esters in alkaline solution. Journal of Pharmaceutical Sciences 1963; 52: 852.10.1002/jps.260052090814061044Search in Google Scholar

[2] Hansch, C., Leo, A., Unger, S. H., Ki Hwan Kim, Nikaitani, D., & Lien, E. J. Aromatic” substituent constants for structure-activity correlations. Journal of Medicinal Chemistry 1973; 16: 1207-1216.10.1021/jm00269a0034747963Search in Google Scholar

[3] Malík, I., Sedlárová, E., Csöllei, J., Račanská, E., Čižmárik, J., & Kurfürst, P. Synthesis, physico-chemical properties and biological activity of 1-(4-fluorophenyl)-4-[3-(2-, 3- and 4-alkyloxyphenylcarbamoyloxy)-2-hydroxypropyl]piperazinium chlorides. Scientia Pharmaceutica 2004; 72: 283-291.10.3797/scipharm.aut-04-24Search in Google Scholar

[4] Malík, I., Sedlárová, E., Andriamainty, F., & Csöllei, J. A study of physicochemical properties of 2-, 3-, 4-alkoxyphenylcarbamic acid derivatives with a substituted N-phenylpiperazine moiety in basic part. (In Slovak) Česka a slovenská farmacie, Czech and Slovak Pharmacy 2005; 54: 235-239.Search in Google Scholar

[5] Malík, I., Sedlárová, E., Csöllei, J., Andriamainty, F., Kurfürst, P., & Vančo, J. (). Synthesis, spectral description, and lipophilicity parameters determination of phenylcarbamic acid derivatives with integrated N-phenylpiperazine moiety in structure. Chemical Papers 2006; 60: 42-47.10.2478/s11696-006-0007-ySearch in Google Scholar

[6] Rácz, I. Drug Formulation. Budapest, Akadémiai Kiadó, 1989; p. 95-104.Search in Google Scholar

[7] Stankovičová, M., Kučárová, M., & Pešák, M. Kinetics of alkaline hydrolysis of substituted esters of phenylcarbamic acid. Chemical Papers 1975; 29: 227-233.Search in Google Scholar

[8] Stankovičová, M., Čižmárik, J., & Pešák, M. Kinetics of alkaline hydrolysis of the 2-piperidinoethyl esters of o-, m-, and p-alkoxyphenylcarbamic acid. Chemical Papers 1978; 32: 86-91.Search in Google Scholar

[9] Stankovičová, M., Bachratá, M., Bezáková, Ž., Blešová, M., Čižmárik, J., & Borovanský, A. Studies of local anaesthetics, LXXXVI. Study of the kinetics of alkaline hydrolysis of carbisocainium chloride, pentacainium chloride and heptacainium chloride. (In Slovak). Česka a slovenská farmacie, Czech and Slovak Pharmacy 1987; 36: 9-15.Search in Google Scholar

[10] Stankovičová, M., Bezáková, Ž., Lukášová-Masná, P., & Lukáš, L. Kinetics of alkaline hydrolysis of potential local anaesthetics - the basic esters of phenylcarbamic acids. Acta Facultatis Pharmaceuticae Universitatis Comenianae 2009; 56: 128-135.Search in Google Scholar

[11] Treindl, Ľ. Chemická kinetika, Chemical Kinetics (in Slovak). Bratislava, Slovak Pedagogical Publishing House, 2nd. ed., 1990; p. 21-22, 73. ISBN 80-08-00365-0.Search in Google Scholar

[12] Waisser, K., Doležal, R., Čižmárik, J., Malík, I., & Kaustová, J. The antimycobacterial derivatives against potential pathogenic strains: 2-Hydroxy-3-(4-phenylpiperazin-1-yl)- propylphenylcarbamates. Scientia Pharmaceutica 2007; 75: 55-61.10.3797/scipharm.2007.75.55Search in Google Scholar