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     ISSN print edition: 0366-6352
ISSN electronic edition: 1336-9075
Registr. No.: MK SR 9/7

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Author: Čižmárik

QSRR modelling aimed on the HPLC retention prediction of dimethylamino- and pyrrolidino-substitued esters of alkoxyphenylcarbamic acid 2525 – 2535
Petra Ranušová, Peter Nemeček, Jozef Lehotay, and Jozef Čižmárik Vol. 75, 6
Application of umbelliferone molecularly imprinted polymer in analysis of plant samples 477 – 483
Katarína Hroboňová, Andrea Spevak, Ľubica Spišská, Jozef Lehotay, and Jozef Čižmárik Vol. 67, 5
Relationship between physicochemical properties, lipophilicity parameters, and local anesthetic activity of dibasic esters of phenylcarbamic acid 206 – 213
I. Malík, E. Sedlárová, J. Csöllei, F. Andriamainty, and J. Čižmárik Vol. 61, 3
Study of Local Anaesthetics, Part 156: Some Physicochemical and Lipophilic Properties of Pyrrolidinoethyl Esters of o-, m-, p-Alkoxy-Substituted Phenylcarbamic Acid 340 – 344
L. Gyurösiová, E. Sedlárová, and J. Čižmárik Vol. 56, 5
Synthesis, Physicochemical Properties, and Conformational Studies of (3-Alkoxymethyl-4-hydroxyphenyl)ethanones 256 – 260
R. Čižmáriková, M. Polakovičová, and E. Mišíková Vol. 56, 4
Neural Network Method, the Tool for Studying Biological Activity of Compounds. Relationship between Infiltration Anaesthesia, Coded Structural Information, and Chromatographic Properties Applied in Homologous Series of Alkoxy-Substituted Esters of Phenylcarbamic Acids 149 – 154
Š. Hatrik, J. Lehotay, and J. Čižmárik Vol. 49, 3
Dimethylaminoethyl Alkoxyphenylcarbamates as Photosynthesis Inhibitors 266 – 268
K. Kráľová, F. Šeršeň, and J. Čižmárik Vol. 46, 4
Ab initio study of geometry and internal rotational barriers of dithiocarbamic acid and several derivatives 151 – 158
M. Remko and J. Čižmárik Vol. 44, 2
Kinetics of alkaline hydrolysis of heptacaine chloride basic analogs 171 – 176
M. Stankovičová, J. Čižmárik, and M. Bachratá Vol. 44, 2
Chromatographic-separation of 3-substituted and 4-substituted anilines and correlation of their Rm values with chosen physicochemical parameters 45 – 52
M. Blešova, J. Čižmárik, and I. Majeríková Vol. 42, 1
Quantum chemical investigations of intermolecular hydrogen bonds formed by phenylcarbamates and N-methylacetamide 577 – 582
M. Remko and J. Čižmárik Vol. 41, 5
1H and 13C nuclear-magnetic-resonance studies of interaction of 5'-AMPwith phenylcarbamate possessing local-anesthetic effect 583 – 592
M. Remko, T. Liptaj, J. Veselovská, and J. Čižmárik Vol. 41, 5
Reactions of hydroxymethylferrocenes with C-acids catalyzed by Ca2+-montmorillonite 747 – 753
Š. Toma, K. Čižmáriková, P. Elečko, and V. Gajda Vol. 40, 6
Study of the synthesis of biaryls on homoionic forms of bentonite or montmorillonite 755 – 761
Š. Toma, K. Čižmáriková, and P. Elečko Vol. 40, 6
Chromatographic parameters of dimethylammonioethyl alkoxycarbanilate chlorides 217 – 224
M. Bachratá, J. Čižmárik, Ž. Bezáková, M. Blešová, and A. Borovanský Vol. 37, 2
Extraction of heptacaine 231 – 235
M. Pešák, F. Kopecký, and J. Čižmárik Vol. 37, 2
Extraction of quaternary ammonium salts of heptacaine 237 – 242
M. Pešák, L. Šlechtová, J. Čižmárik, A. Borovanský, and P. Švec Vol. 37, 2
Preparation and spectral properties of cyclic acetals of 2,2,5,5-tetrakis(hydroxymethyl)cyclopentanone 213 – 222
R. Čižmáriková and J. Heger Vol. 34, 2
Cryoscopic properties of aqueous solutions of heptacaine and some of its analogs 42 – 50
F. Kopecký, V. Záhorka, M. Vojteková, and J. Čižmárik Vol. 32, 1
Kinetics of alkaline hydrolysis of the 2-piperidinoethyl esters of o-, m-, and p-alkoxyphenylcarbamic acids 86 – 91
M. Stankovičová, J. Čižmárik, and M. Pešák Vol. 32, 1
Study of the reaction products of 2,2,5,5-tetrakis(halomethyl)cyclopentanone with potassium cyanide 92 – 99
R. Čižmáriková and J. Heger Vol. 32, 1
Reactions of 5,6-dihydro-4,7-dithia-1,3-indandione with aldehydes and ketones 836 – 842
P. Hrnčiar and R. Čižmáriková Vol. 29, 6
Synthesis, uv and i.r. spectra of 2-piperidinoethyl esters of alkyloxyphenylcarbamic acids 119 – 123
J. Čižmárik and A. Borovanský Vol. 29, 1

Tuesday, September 29, 2026

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