Calculations of electrostatic potential maps and atomic charges for large molecules,
J. Chem. Inf. Comp. Sci. 33, 296 (1993).
Gas chromatographic-mass spectrometric determination of a-phenylcinnamic acid isomers: practical and theoretical aspects,
J. Chromat. A 668, 353 (1994).
Using molecular electrostatic potential maps for similarity studies,
Top. Curr. Chem. 174, 45 (1995).
Bond order calculations on neutral molecules and radical cations: Predicting fragmentation patterns a-phenylcinnamic acid silylesters on electron impact ionization
QSAR and Molecular Modelling: Concepts and Biological Applications (Eds. Sanz, F., Giraldo, J., Manaut, F.) p. 305 Prous Science Publishers, Barcelona, 1995.
Experimental and computational tools for mechanistic study: a modified Perkin condensation leading to a-phenylcinnamic acid isomers,
E(lectronic) C(onference on) T(rends in) O(rganic) C(hemistry), CD-ROM (Eds. Rzepa, H.S., Leach, C., Goodman, J.M.), The Royal Society of Chemistry, 1996, ISBN 08540 4 899 5 (http://www.ch.ic.ac.uk/ ectoc/papers/).
Rearrangement reactions an EI ionization of aphenylcinnamic acid trimethylsilyl esters; Oractical and theoretical aspects,
J. Mass Spect. 31, 823 (1996).
Structure and isomerization of a-phenylcinnamic acid stereoisomers - reaction pathway and transition-state structure by semiempirical methods,
J. Mol. Struct. THEOCHEM 391, 189 (1997).
Protonation and ring closure of stereoisomeric a-substituted cinnamic acids in superacidic media studied by 13C NMR spectroscopy and computations,
J. Chem. Soc., Perkin Trans. 2 379 (1998).
Fragmentation of cyclobutane derivatives upon Electron Impact: Transformation pathways elucidated by mass spectrometric methods and semi-empirical quantum chemical calculations,
Rapid Commun. Mass Spectrom. 12, 1771 (1998).
Molecular electrostatics, energetics and dynamics of the alkylation of naphthalane: Positional isomerization of monoalkylnaphthalenes at Hartree-Fock and correlated levels with BSSE-corrections,
J. Phys. Chem. A 104, 1337 (2000).
Synthesis of E- and Z-o-methoxy-substituted 2,3-diphenyl propenoic acids and its methyl esters,
Synth. Commun. 30, 1543 (2000).
The role of ammonium salts in the oxidation of hydrocarbons by O2 catalysed by cationic phase-transfer reagents,
PCCP 2, 3801 (2000).
On the mechanism of a modified Perkin condensation leading to a-phenylcinnamic acid stereoisomers - experiments and molecular modeling,
Monatsh. Chem. 131, 1097 (2000).
Combined computational and experimental investigations on the diastereoselective hydrogenation of steroids by chiral oxazaborolidine,
Int. J. Quant. Chem. 84, 253 (2001).
Preparation of new 2,3-diphenylpropenoic acid esters - good yields even for the more hindered Z isomers,
Molecules 9, 256 (2004).
Preparation of 3-substituted and 2,3-disubstituted-4,4,4-trifluoro-2-butenoic acids Perkin condensation of activated aromatic ketones,
J. Fluorine Chem. 126, 850 (2006).
The cis-trans isomerisation of homologous 2-hydroxycycloalkanecarboxylic acids under basic conditions,
Chin. J. Chem. 24,1792 (2006).
Onium salts as catalysts in the liquid-phase oxidation of cyclohexene or tetraline by N2O,
Proc. 9th Pannonian Int. Symp. Catal., trbské pleso (Slovakia), 2008, 381-387.
Comments on "Shape-selective diisopropylation of naphthalene in H-mordenite: Myth or reality?"
J. Catal. 279, 229 (2011).