about
Bile acid amidoalcohols: simple organogelators.Structural, thermoanalytical and molecular modeling studies on N-(3-hydroxypropyl) 3 alpha,12 alpha-dihydroxy-5 beta-cholan-24-amide and its monohydrates.Crystal structures of 2,2'-bipyridin-1-ium 1,1,3,3-tetracyano-2-ethoxyprop-2-en-1-ide and bis(2,2'-bipyridin-1-ium) 1,1,3,3-tetracyano-2-(dicyanomethylene)propane-1,3-diideN-[2-(2,2-Di-methyl-propanamido)-pyrimidin-4-yl]-2,2-di-methyl-propanamide n-hexane 0.25-solvate hemihydrate.6-Amino-2-(pivaloyl-amino)-pyridinium benzoate.N,N,N,N-Tetra-kis(2,3,4,5,6-penta-fluoro-benzo-yl)pyridine-2,6-diamine.cis,cis,cis-(Acetato-κ(2) O,O')bis-[1,2-bis-(diphenyl-phosphan-yl)ethane-κ(2) P,P']ruthenium(II) 0.75-trifluoro-methane-sulfonate 0.25-chloride.Synthesis and structural characterization of substituted 2-phenacylbenzoxazoles.(E)-7-(Pyren-1-yl)hept-6-enoic acid.N-Benzyl-2,3,4,5,6-penta-fluoro-benz-amide.2-Methyl-4-phenyl-3,4-dihydro-quinazoline.Crystal structure of [tris-(4,4'-bi-pyridine)]-diium bis-(1,1,3,3-tetra-cyano-2-eth-oxy-propenide) trihydrate.The pentafluorophenyl group as π-acceptor for anions: a case study.Efficient stabilisation of a dihydrogenphosphate tetramer and a dihydrogenpyrophosphate dimer by a cyclic pseudopeptide containing 1,4-disubstituted 1,2,3-triazole moieties.3α-Hydr-oxy-N-(3-hydroxy-prop-yl)-5β-cholan-24-amide.2-exo,5-endo,8,8,10-Penta-chloro-bornane.Non-centrosymmetric tetrameric assemblies of tetramethylammonium halides with uranyl salophen complexes in the solid state.Self-organization of 2-acylaminopyridines in the solid state and in solution.Bile acid-derived mono- and diketals--synthesis, structural characterization and self-assembling properties.CH-directed anion-pi interactions in the crystals of pentafluorobenzyl-substituted ammonium and pyridinium salts.Piperazine bridged resorcinarene cages.Crystal structure of 2-methyl-piperazine-1,4-diium bis-(hydrogen maleate).Substituent effect in 2-benzoylmethylenequinoline difluoroborates exhibiting through-space couplings. Multinuclear magnetic resonance, X-ray diffraction, and computational study.Association of N-(pyridin-2-yl),N'-substituted ureas with 2-amino-1,8-naphthyridines and benzoates: NMR and quantum chemical studies of the substituent effect on complexation.2-Acylamino- and 2,4-bis(acylamino)pyrimidines as supramolecular synthons analyzed by multiple noncovalent interactions. DFT, X-ray diffraction, and NMR spectral studies.Molecular aggregation in selected crystalline 1:1 complexes of hydrophobic D- and L-amino acids. IV. The L-phenylalanine series.Long-range atmospheric transport of three toxaphene congeners across Europe. Modeling by chained single-box FATEMOD program.Chasing Weak Forces: Hierarchically Assembled Helicates as a Probe for the Evaluation of the Energetics of Weak Interactions.Squaramide-Catalyzed Asymmetric aza-Friedel-Crafts/N,O-Acetalization Domino Reactions Between 2-Naphthols and Pyrazolinone Ketimines.Coordinatively Unsaturated Lanthanide(III) Helicates: Luminescence Sensors for Adenosine Monophosphate in Aqueous Media.Oxoanion binding to a cyclic pseudopeptide containing 1,4-disubstituted 1,2,3-triazole moieties.Achieving Strong Positive Cooperativity through Activating Weak Non-Covalent Interactions.An aryl-fused redox-active tetrathiafulvalene with enhanced mixed-valence and radical-cation dimer stabilities.Asymmetric Synthesis of Functionalized Tricyclic Chromanes via an Organocatalytic Triple Domino Reaction.Crystal Structures and Cytotoxicity of ent-Kaurane-Type Diterpenoids from Two Aspilia SpeciesA conformationally adaptive macrocycle: conformational complexity and host-guest chemistry of zorb[4]arene.Bis(6-thioxo-1,6-dihydropurinium) tetrachlorozincate(II)A novel caryophyllene type sesquiterpene lactone from Asparagus falcatus (Linn.); structure elucidation and anti-angiogenic activity on HUVECsMicrowave assisted synthesis and solid-state characterization of lithocholyl amides of isomeric aminopyridinesConcerted halogen and hydrogen bonding in [RuI2(H2dcbpy)(CO)2]···I2···(CH3OH)···I2···[RuI2(H2dcbpy)(CO)2]
P50
Q30976823-4A8F7609-608B-4C0D-B7C5-8DBED52EB940Q31134314-66AEBF5E-C0E0-4022-B8C4-24EE6952FA60Q35570756-8616F5C7-3CB7-4701-A932-10C27D5FC046Q37447321-D2C61CD8-7F99-4057-B7CD-E36157021783Q37447960-CC94BECF-EB57-4572-8AED-78C2323E5FDEQ39822624-B424AF7A-DB58-466E-80AA-7A902BED1511Q39924550-0B560619-076A-44A2-AFE3-C8CFC6E0AB65Q40042472-6FCFF1AF-5424-4DA8-B567-EBD65C8496B6Q41354810-9C3EFAE0-4F2F-450E-93DC-35AA23E3A72FQ41445203-A49D629B-E1EC-4AC8-8D50-3D1E020440D6Q41933570-9B7648AE-8400-4C5B-A2F3-CB22EF2BBC5AQ42177780-6C1E209C-4027-4405-B401-F018A4DFDD96Q42354376-5DA52BD0-3A37-4F95-B644-D8A29D045CA6Q42367175-DA721F61-F0B1-4ABF-94ED-BBA8534F3220Q42389882-AA2C91D8-5E4C-4D9A-970F-8D0F32A15448Q42403871-D54B9F5E-4E1C-4A73-968D-0160F9BC1966Q42797168-06D24B53-10CD-4E9F-9E62-B852CF2893BFQ42920543-93F04414-CD70-4323-896C-E7512F99BBE3Q43098909-98EDF5D6-E91B-42B0-87D6-1167D3965120Q43116063-66E38D5C-B1FD-4CC7-B7A9-960C793E8DFBQ43141888-DF339BBC-63CB-4B53-B325-477E57638882Q43177475-F913DBAB-8E47-4974-AA26-E4BE08B25C17Q44028842-3C342335-3CBE-4E14-8673-4874D6397558Q44277224-041731D6-D929-435D-85D4-A69E7FA2798DQ44513863-15C805D5-5E67-45F3-B06E-C9ED8EE39E45Q45981959-8A179E3A-B173-4BC0-80E8-4DB3BBBD1D37Q46170312-5B900045-E335-442B-814D-8689A9E0EF39Q48129496-C48B35D9-3100-4276-8D34-EF3F07F82A93Q48167844-EAC36EB8-DD63-4ADF-A33D-9D168818F16DQ48185112-49582F62-2427-4487-8D27-00D0DA79D70FQ48253051-D46619B1-E30F-4690-8607-6D5B662E9303Q48302036-D01A0E83-2B70-4C1A-812A-CF0EE9FF2919Q52624024-7F7DB783-2666-4FB1-B6F0-D7484CB7DF42Q54725108-AC9DAA7F-2A9F-4CA6-AC76-C9F1B1D14E5DQ60919844-2A87F2C6-BCEC-45FB-B138-A2F8868EA7DBQ64896434-884236D9-1938-4802-ACDF-7294164BA123Q79845318-89B6E4D8-8C77-4C89-97A4-669FC77A181EQ82461293-D90AA9E0-9D2C-417E-BDF2-B51579062C20Q82734443-EAFF1F37-7D6F-4134-A0D2-1545515D4C01Q83346489-65254632-8093-473E-9748-C59B8EC38A2F
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Arto Valkonen
@ast
Arto Valkonen
@en
Arto Valkonen
@es
Arto Valkonen
@nl
type
label
Arto Valkonen
@ast
Arto Valkonen
@en
Arto Valkonen
@es
Arto Valkonen
@nl
prefLabel
Arto Valkonen
@ast
Arto Valkonen
@en
Arto Valkonen
@es
Arto Valkonen
@nl
P106
P31
P496
0000-0003-2806-3807