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Csizmadia I. G.
Csizmadia Imre G.
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I. G.
Imre G.
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http://hub.abes.fr/acs/periodical/jacsat/1975/volume_97/issue_18/101021ja00851a032/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1979/volume_101/issue_5/101021ja00499a003/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1991/volume_113/issue_16/101021ja00016a049/authorship/7
http://hub.abes.fr/acs/periodical/jacsat/1966/volume_88/issue_11/101021ja00963a009/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_15/101021ja0585127/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1976/volume_98/issue_16/101021ja00432a016/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1987/volume_109/issue_8/101021ja00242a001/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1975/volume_97/issue_8/101021ja00841a036/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1972/volume_94/issue_24/101021ja00779a006/authorship/4
http://hub.abes.fr/acs/periodical/jpcafh/2004/volume_108/issue_38/101021jp0403240/authorship/5
http://hub.abes.fr/acs/periodical/jpcafh/2003/volume_107/issue_25/101021jp030111v/authorship/6
http://hub.abes.fr/acs/periodical/jpcafh/2006/volume_110/issue_18/101021jp058215o/authorship/5
http://hub.abes.fr/acs/periodical/jpcafh/2005/volume_109/issue_11/101021jp040594i/authorship/9
http://hub.abes.fr/acs/periodical/jpcafh/2005/volume_109/issue_24/101021jp040720i/authorship/12
http://hub.abes.fr/acs/periodical/jpcafh/2002/volume_106/issue_43/101021jp021253c/authorship/7
http://hub.abes.fr/acs/periodical/jpcafh/2003/volume_107/issue_29/101021jp030057i/authorship/8
http://hub.abes.fr/acs/periodical/jpcafh/2006/volume_110/issue_40/101021jp0680488/authorship/5
http://hub.abes.fr/acs/periodical/jpcafh/2005/volume_109/issue_3/101021jp040546y/authorship/4
http://hub.abes.fr/acs/periodical/jpcafh/2002/volume_106/issue_30/101021jp014514b/authorship/8
http://hub.abes.fr/acs/periodical/jpcafh/2006/volume_110/issue_49/101021jp065595k/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/2001/volume_123/issue_25/101021ja0038934/authorship/7
http://hub.abes.fr/acs/periodical/jpcafh/2004/volume_108/issue_29/101021jp040196f/authorship/4
http://hub.abes.fr/acs/periodical/jpcafh/2006/volume_110/issue_10/101021jp058219t/authorship/3
http://hub.abes.fr/acs/periodical/jpcafh/2000/volume_104/issue_15/101021jp9935034/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1975/volume_97/issue_8/101021ja00841a005/authorship/3
http://hub.abes.fr/acs/periodical/jpchax/1986/volume_90/issue_2/101021j100274a015/authorship/7
http://hub.abes.fr/acs/periodical/jacsat/1976/volume_98/issue_6/101021ja00422a079/authorship/5
http://hub.abes.fr/acs/periodical/jpchax/1984/volume_88/issue_13/101021j150657a046/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1967/volume_89/issue_22/101021ja00998a042/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1973/volume_95/issue_1/101021ja00782a022/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1978/volume_100/issue_22/101021ja00490a023/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1995/volume_117/issue_5/101021ja00110a028/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/1993/volume_115/issue_11/101021ja00064a053/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1970/volume_92/issue_22/101021ja00725a001/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/1968/volume_90/issue_26/101021ja01028a041/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1993/volume_115/issue_18/101021ja00071a046/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/1974/volume_96/issue_13/101021ja00820a023/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1993/volume_115/issue_18/101021ja00071a041/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/1977/volume_99/issue_14/101021ja00456a001/authorship/2
http://hub.abes.fr/springer/periodical/214/1993/volume_85/issue_1_3/B8ECE60F19B86116E053120B220A89FA/authorship/3
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of
The Reactions of Sulfur Atoms. VII. The Ultraviolet Spectrum, the Photolysis, and the Mercury Sensitization of Carbonyl Sulfide
Mechanism of the Wolff rearrangement. 6. Ab initio molecular orbital calculations on the thermodynamic and kinetic stability of the oxirene molecule
A systematic study of the ionization potentials and electron, proton, hydrogen, and hydride affinities of OHn molecules and ions
Mercury 6(3P1) photosensitization of mono- and difluoroethylenes. Correlation of mechanism with calculated molecular orbital energy levels
Reactions of sulfur atoms. XIV. Ab initio molecular orbital calculations on the ethylene episulfide molecule and the S + C2H4 reaction path
Irrelevance of d-orbital conjugation. I. .alpha.-Thiocarbanion. Comparative quantum chemical study of the static and dynamic properties and proton affinities of carbanions adjacent to oxygen and to sulfur
Analysis of the topological features of the conformational hypersurface of n-butane
Use of a modified Romberg formalism for the extrapolation of molecular properties from oligomers to polymers. Polyalanine diamide in its (.gamma.L)n or (C7)n conformation
Peptide models II. Intramolecular interactions and stable conformations of glycine, alanine, and valine peptide analogues
Mechanism of the Wolff rearrangement
Ab initio study of methylcarbene and the stereochemistry of its rearrangement to ethylene
Stereochemistry of carbene rearrangements. Correlation of ab initio molecular orbitals as an aid to the investigation of the electron redistribution mechanism
Nonempirical molecular orbital calculations on an .alpha.-sulfinyl carbanion
Ab Initio Study of Lowest-Energy Conformers of Lewis X (Lex) Trisaccharide
Thermodynamic Functions of Conformational Changes. 2. Conformational Entropy as aMeasure of Information Accumulation
Molecular Study on the Enantiomeric Relationships of Carvedilol Fragment A,4-(2-Hydroxypropoxy)carbazol, along with Selected Analogues
Pharmacophore Fragment-Based Prediction and Gas-Phase ab Initio Optimization ofCarvedilol Conformations
Resolution of Carvedilol's Conformational Surface via Gas and Solvent Phase DensityFunctional Theory Optimizations and NMR Spectroscopy
Folded and Unfolded Conformations of the ω-3 Polyunsaturated Fatty Acid Family: CH3CH2[CHCHCH2]B[CH2]MCOOH. First Principles Study
α- and 310-Helix Interconversion: A Quantum-Chemical Study onPolyalanine Systems in the Gas Phase and in Aqueous Solvent
Exploration of the Four-Dimensional-Conformational Potential Energy Hypersurface ofN-Acetyl-l-aspartic Acid N‘-Methylamide with Its Internally Hydrogen Bonded Side-ChainOrientation
Characterization of the Conformational Probability of N-Acetyl-Phenylalanyl-NH2 by RHF,DFT, and MP2 Computation and AIM Analyses, Confirmed by Jet-Cooled Infrared Data
Flexibility of “Polyunsaturated Fatty Acid Chains” and Peptide Backbones: A Comparativeab Initio Study
First-Principle Computational Study on the Full Conformational Space of l-ThreonineDiamide, the Energetic Stability of Cis and Trans Isomers
Exploration of the Full Conformational Space of N-Acetyl-l-glutamine-N-methylamide. Anab Initio and Density Functional Theory Study
Density Functional Molecular Study on the Full Conformational Space of theS-4-(2-Hydroxypropoxy)carbazol Fragment of Carvedilol (1-(9H−Carbazol-4-yloxy)-3-[2-(2-methoxyphenoxy)ethylamino]-2-propanol) in Vacuum and in Different Solvent Media
Theoretical Study on Tertiary Structural Elements ofβ-peptides: Nanotubes Formed from Parallel-Sheet-DerivedAssemblies of β-Peptides
First Principle Computational Study on the Full Conformational Space of l-ProlineDiamides
Thermodynamic Functions of Conformational Changes: Conformational Network ofGlycine Diamide Folding, Entropy Lowering, and Informational Accumulation
Bonding between nonbonded sulfur and oxygen atoms in selected organic molecules (a quantum chemical study)
Peptide models. 1. Topology of selected peptide conformational potential energy surfaces (glycine and alanine derivatives)
PEPTIDE MODELS. 17. The role of the water molecule in peptide folding. An ab initio study on the right-handed helical conformations of N-formylglycinamide and N-formyl-L-alaninamide monohydrates [H(CONH-CHR-CONH)H.H2O; R = H or CH3]
The ground electronic state of silaethylene. An ab initio molecular orbital study of the lower electronic manifold
Peptide models 6. New .beta.-turn conformations from ab initio calculations confirmed by x-ray data of proteins
Peptide models. 3. Conformational potential energy hypersurface of formyl-L-valinamide
Mechanism of the Wolff rearrangement. V. Semiempirical molecular orbital calculations on .alpha.-diazo ketones, oxirenes, and related reaction intermediates
Chemical dynamics of symmetric and asymmetric reaction coordinates
Theoretical Study on the CuH (copper hydride) + H (atomic hydrogen) -> Cu (copper) + H2 (molecular hydrogen) reaction pathway
Determination and analysis of the formic acid conformational hypersurface
Ab initio self-consistent field calculations of lithium atom insertion into a carbon-hydrogen bond of methane
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