about
Design of stereoelectronically promoted super lewis acids and unprecedented chemistry of their complexes.NMR determination of pKa values of indoloquinoline alkaloids.Loss of loop adenines alters human telomere d[AG3(TTAG3)3] quadruplex folding.Anion-π Interactions in Flavoproteins Involve a Substantial Charge-Transfer Component.Quaternary protoberberine alkaloids.Natural compound cudraflavone B shows promising anti-inflammatory properties in vitro.Cytotoxic activities of several geranyl-substituted flavanones.High-Frequency (13)C and (29)Si NMR Chemical Shifts in Diamagnetic Low-Valence Compounds of Tl(I) and Pb(II): Decisive Role of Relativistic Effects.Intermolecular Interactions in Crystalline Theobromine as Reflected in Electron Deformation Density and (13)C NMR Chemical Shift Tensors.All-Metal Aromaticity: Revisiting the Ring Current Model among Transition Metal Clusters.Chemoprotective and toxic potentials of synthetic and natural chalcones and dihydrochalcones in vitro.Structure, solvent, and relativistic effects on the NMR chemical shifts in square-planar transition-metal complexes: assessment of DFT approaches.Interpretation of indirect nuclear spin-spin couplings in isomers of adenine: novel approach to analyze coupling electron deformation density using localized molecular orbitals.1H-, 13C-, and 15N-NMR chemical shifts for selected glucosides and ribosides of aromatic cytokinins.Extractions of isoquinoline alkaloids with butanol and octanol.13C chemical shift tensors in hypoxanthine and 6-mercaptopurine: effects of substitution, tautomerism, and intermolecular interactions.A relativistic DFT methodology for calculating the structures and NMR chemical shifts of octahedral platinum and iridium complexes.Origin of the conformational modulation of the 13C NMR chemical shift of methoxy groups in aromatic natural compounds.Palmatine and berberine isolation artifacts.Understanding the NMR chemical shifts for 6-halopurines: role of structure, solvent and relativistic effects.Interpretation of substituent effects on 13C and 15N NMR chemical shifts in 6-substituted purines.Toward a consistent interpretation of the QTAIM: tortuous link between chemical bonds, interactions, and bond/line paths.129Xe NMR chemical shift in Xe@C60 calculated at experimental conditions: essential role of the relativity, dynamics, and explicit solvent.Electron density shift in imidazolium derivatives upon complexation with cucurbit[6]uril.Covalent bonding of azoles to quaternary protoberberine alkaloids.Synthesis and structure-activity relationship studies of theophylline analogs on population responses in the rat hippocampus in vitro.Theoretical and experimental NMR study of protopine hydrochloride isomers.Modulating Electron Sharing in Ion-π-Receptors via Substitution and External Electric Field: A Route toward Bond Strengthening.Antibacterial C-geranylflavonoids from Paulownia tomentosa Fruits.Experimental and quantum-chemical studies of 15N NMR coordination shifts in palladium and platinum chloride complexes with pyridine, 2,2'-bipyridine and 1,10-phenanthroline.Potential energy surface and binding energy in the presence of an external electric field: modulation of anion-π interactions for graphene-based receptors.Water-tryptophan interactions: lone-pair---pi or O-H---pi? Molecular dynamics simulations of beta-galactosidase suggest that both modes can co-exist.Hyperfine Effects in Ligand NMR: Paramagnetic Ru(III) Complexes with 3-Substituted Pyridines.Modified Guanines as Constituents of Smart Ligands for Nucleic Acid Quadruplexes.Supramolecular Covalence in Bifurcated Chalcogen Bonding.Weak Supramolecular Interactions Governing Parallel and Antiparallel DNA Quadruplexes: Insights from Large-Scale Quantum Mechanics Analysis of Experimentally Derived Models.Solvent effects on ion-receptor interactions in the presence of an external electric field.Anti-Electrostatic CH-Ion Bonding in Decorated Graphanes.Linking the Character of the Metal-Ligand Bond to the Ligand NMR Shielding in Transition-Metal Complexes: NMR Contributions from Spin-Orbit Coupling.How Does a Container Affect Acidity of its Content? Charge-Depletion Bonding Inside Fullerenes.
P50
Q30838205-EDDE3BD4-7AEF-40D7-AAAC-17494C7ACFF5Q33490188-78A4E4B3-BBBB-47FD-AC72-A9DBC59D5A53Q34712068-9D23A429-52B8-45C8-9BBE-6F1E80DECD29Q36252362-E0963883-1CA2-4670-BBCA-16F357D04FBCQ36655345-8220FFFD-3289-4984-A10F-3868BA3BE20FQ39592612-143EE25E-23C9-47D4-BCB4-6986C0E6D86FQ39733849-99E0D66B-2D40-4B44-9736-EBBE74BA8A99Q40050005-A2414998-16F6-43E9-B5B2-DDAEE39EC969Q40303533-E29D0C1A-FAD6-43CA-A51B-4BD033472DE7Q40304715-8CB9E7A0-F9B9-4B0F-B1E8-430D90CD9F4FQ40467745-F846FF2F-9067-4E44-8798-3D82055D9D36Q40567690-34B7566D-6AFF-42AF-A348-43AC640909D6Q43046586-26DEC8FF-41AF-4020-B0E5-5941819999AAQ43144370-ED51E066-F194-45F5-9A5B-E2A8B0908044Q43179718-682CD5E8-9A03-4E69-9884-B2622EE16E6AQ43200601-E6DC5DE2-E97B-475A-8761-3A5E1A072D47Q43655859-264DE635-11DF-441A-B191-275A835C7C96Q43696860-CFA6B2B7-A958-4198-8283-643EDF0B0BF5Q44416165-A1A41EBD-2E66-41BC-AE25-42057073862CQ44550977-582604B7-C32B-42AC-B81B-C1FC5CE3F5E2Q44909911-2DA3297D-E86C-477F-B49F-FC1B187CA812Q45221702-04E39AAF-2E76-43C6-B3B3-30ABC7D3BBFCQ45899387-0308BE3F-40E6-44EB-98FD-C308A6C97451Q45975118-B196570F-4008-458B-BC07-12DC1202DD00Q46378394-4466F2D8-EC58-475A-AA6E-A180B5EDFE6DQ46448581-A9A26CD5-7614-473D-9854-DF94A746DA14Q46482077-1329F19B-5441-40AD-87B4-01053AA3AEE0Q46525219-5980C06A-DC1B-4A5D-9757-DD13E487EEB3Q46738653-0918011F-2DF7-4721-8F13-B7311BDA750EQ46878745-ED9FAC20-45E1-4B97-9006-2672D9BBF742Q46956268-525935AE-2C55-4675-A6E1-779534BA48E2Q47217907-06FDFB8B-A679-4075-A462-1BE19C84AE48Q47398503-C9FA77B5-3042-4403-BBEE-D33B2B2A8568Q48041585-D771AC6F-DCCD-4D86-8F09-97498E3D89FCQ48044981-DED73AAE-B6C5-429F-A5CF-CC512E920315Q48046729-D49BC049-675D-4A93-B85D-B1D6E76E483BQ48053537-4EF96BBC-BAD1-4C32-8929-14054300D6DAQ48056802-3AE0097E-65BB-42F0-A337-8F9D46BA4AABQ48058307-6BD732C4-1B6A-476E-AFDF-99043F5473ACQ50068757-1B80BC32-6A72-4315-A5A4-15AC86A57354
P50
description
hulumtues
@sq
researcher
@en
ricercatore
@it
wetenschapper
@nl
հետազոտող
@hy
name
Radek Marek
@ast
Radek Marek
@cs
Radek Marek
@en
Radek Marek
@es
Radek Marek
@nl
Radek Marek
@sl
type
label
Radek Marek
@ast
Radek Marek
@cs
Radek Marek
@en
Radek Marek
@es
Radek Marek
@nl
Radek Marek
@sl
prefLabel
Radek Marek
@ast
Radek Marek
@cs
Radek Marek
@en
Radek Marek
@es
Radek Marek
@nl
Radek Marek
@sl
P214
P106
P1153
7003918548
P21
P214
P31
P496
0000-0002-3668-3523
P569
1967-12-10T00:00:00Z
P691
P734
P735
P7859
viaf-90622480