about
An effective simulation of aqueous micellar aggregates by computational models.Nitrosonium complexes of resorc[4]arenes: spectral, kinetic, and theoretical studies.Effect of ring size on the tautomerization and ionization reaction of cyclic 2-nitroalkanones: an experimental and theoretical study.Stereodynamic investigation of labile stereogenic centres in dihydroartemisinin.3-(Phenyl-4-oxy)-5-phenyl-4,5-dihydro-(1H)-pyrazole: A fascinating molecular framework to study the enantioseparation ability of the amylose (3,5-dimethylphenylcarbamate) chiral stationary phase. Part II. Solvophobic effects in enantiorecognition pr2-(Alkyl/aryl)amino-6-benzylpyrimidin-4(3H)-ones as inhibitors of wild-type and mutant HIV-1: enantioselectivity studies.3-(Phenyl-4-oxy)-5-phenyl-4,5-dihydro-(1H)-pyrazole: A fascinating molecular framework to study the enantioseparation ability of the amylose (3,5-dimethylphenylcarbamate) chiral stationary phase. Part I. Structure-enantioselectivity relationships.Enantiomers of triclabendazole sulfoxide: Analytical and semipreparative HPLC separation, absolute configuration assignment, and transformation into sodium salt.Basicity of pyridine and some substituted pyridines in ionic liquids.Transition from enantioselective high performance to ultra-high performance liquid chromatography: A case study of a brush-type chiral stationary phase based on sub-5-micron to sub-2-micron silica particles.Towards enzyme-like enantioselectivity in the gas phase: conformational control of selectivity in chiral macrocyclic dimers.Conformational studies by dynamic NMR. 86. Structure, stereodynamics, and cryogenic enantioseparation of the stereolabile isomers of o-dinaphthylphenyl derivatives.Conformational studies by dynamic NMR. 89. Stereomutation and cryogenic enantioseparation of conformational antipodes of hindered aryl oximes.Enantiomerization study of some alpha-nitroketones by dynamic high-resolution gas chromatography.Efficient organic monoliths prepared by γ-radiation induced polymerization in the evaluation of histone deacetylase inhibitors by capillary(nano)-high performance liquid chromatography and ion trap mass spectrometry.Stereolability of dihydroartemisinin, an antimalarial drug: a comprehensive thermodynamic investigation. Part 1.Enantiomers of C(5)-chiral 1-acetyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives: Analytical and semipreparative HPLC separation, chiroptical properties, absolute configuration, and inhibitory activity against monoamine oxidase.Influence of the nature of alkyl substituents on the high-performance liquid chromatography enantioseparation and retention of new atropisomeric 1,1'-bibenzimidazole derivatives on amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase.Solvent effects on the rate of the keto-enol interconversion of 2-nitrocyclohexanone.Dynamic HPLC of stereolabile iron(II) complexes on chiral stationary phases.Enantiomerization of chiral uranyl-salophen complexes via unprecedented ligand hemilability: toward configurationally stable derivatives.On-column epimerization of dihydroartemisinin: an effective analytical approach to overcome the shortcomings of the International Pharmacopoeia monograph.A rational approach to predict and modulate stereolability of chiral alpha substituted ketones.Exceptional gas-phase enantioselectivity of chiral tetramide macrocycles.Stereolability of chiral ruthenium catalysts with frozen NHC ligand conformations investigated by dynamic-HPLC.Stereomutations of atropisomers of sterically hindered salophen ligands.Determination of the polarities of some ionic liquids using 2-nitrocyclohexanone as the probe.Induced-fit in the gas phase: conformational effects on the enantioselectivity of chiral tetra-amide macrocycles.High-performance liquid chromatographic separation of enantiomers and diastereomers of 2-methylcyclohexanone thiosemicarbazone, and determination of absolute configuration and configurational stability.Ultra-fast high-efficiency enantioseparations by means of a teicoplanin-based chiral stationary phase made on sub-2 μm totally porous silica particles of narrow size distribution.Dynamic high performance liquid chromatography on chiral stationary phases. Low temperature separation of the interconverting enantiomers of diazepam, flunitrazepam, prazepam and tetrazepam.Stereolability of dihydroartemisinin, an antimalarial drug: a comprehensive kinetic investigation. Part 2.Determination of the Enantiomerization Barrier of the Residual Enantiomers of C3 -Symmetric Tris[3-(1-Methyl-2-Alkyl)Indolyl]Phosphane Oxides: Case Study of a Multitasking HPLC Investigation Based on an Immobilized Polysaccharide Stationary Phase."Inherently Chiral" Ionic-Liquid Media: Effective Chiral Electroanalysis on Achiral Electrodes.3-methylcyclohexanone thiosemicarbazone: determination of E/Z isomerization barrier by dynamic high-performance liquid chromatography, configuration assignment and theoretical study of the mechanisms involved by the spontaneous, acid and base catalyIonization and tautomerization of 2-nitrocyclohexanone in aqueous solution."Quasi flexible" automatic docking processing for studying stereoselective recognition mechanisms, part 2: Prediction of DeltaDeltaG of complexation and 1H-NMR NOE correlation.Recognition mechanism of aromatic derivatives resolved by argentation chromatography: The driving role played by substituent groups.Steric and electronic effects on the configurational stability of residual chiral phosphorus-centered three-bladed propellers: tris-aryl phosphane oxides.Steric and electronic effects on the configurational stability of residual chiral phosphorus-centered three-bladed propellers: tris-aryl phosphanes.
P50
Q31004695-CE4D970D-1EEF-4500-AE06-E669BFCD163CQ31122036-1E32EAC9-E3FF-4EA0-B650-AC61CBC9F602Q34101810-A97B3889-676A-4060-884E-68E56B574A72Q37718549-702CE361-2886-45AA-87EA-CF4CBB1C7A1EQ38833794-154A07B2-4DDC-4CF3-8DF1-455080FAFF58Q39377246-AFD2614D-CB73-4765-9495-E5040B2AE292Q39556209-01B47BF9-FF02-4E15-B280-E7E46959E427Q40275002-595E53EC-7F44-40B9-A973-8C98D324B392Q43076228-A3143A13-E21B-402B-9541-1D580AC43C0FQ43252378-E806AF95-1D82-445D-9805-4397E83B39D5Q43282253-5966852A-5C68-47BE-A398-59C0964A3255Q43901001-435E94D3-5FBD-4B2C-9A7B-A3EF6B22CC60Q43970756-A1652BDD-BEF0-482D-B242-A7F4659AA8C3Q44399308-901B1B94-0BD2-4ED2-9256-FB148F4FC17FQ44519360-196B8608-2B1E-475D-9D81-CFA5A4A6A69DQ44665691-276CBED1-53BB-42EF-B616-46F7B2BA256FQ45070123-DDF2AE9F-A829-4121-B383-58D6D68D171BQ45879351-31B2B9F5-E40B-46D7-B414-64EA42608235Q46274990-3A41B9FE-5786-417F-9ADA-32656D8809CFQ46462952-74CA3CA9-0B3D-4024-99DD-CF62A5CD2BE3Q46481288-48327657-600B-498B-974C-DB2A540618A3Q46490535-7D7ADAF2-D9C2-4746-9016-F2987A3C00C5Q46540617-0CF43574-96DA-49EC-8A71-DB4AA1A1E85BQ46665222-0D721989-BBD9-46DF-8160-AB47339E5D06Q46687870-86ADD356-57C3-4816-B234-255A9A33F410Q46764901-B9088D7C-795C-4E3C-8346-ED3619559F4FQ46796201-BA68D0AB-5284-4DB5-8F88-DF31CC1EE304Q46839428-61BB1B04-94C2-4D87-928E-F8ED65EC7A11Q46933344-98046A62-9056-4A04-889F-F5A6418F2A3BQ47338727-2E0AC0F0-48F3-489D-A893-84489C276409Q47827260-7F0B12DA-C986-490A-8DB5-955FE8059541Q47979173-0924C119-B9C1-426A-A39D-9E9433B449B0Q48129253-07D3A52A-3209-45D0-8B61-459F7573F5E2Q48341973-7CF852FA-95B2-41D9-A3FF-B112A192B1E4Q49093339-747C3E83-1838-4590-86DD-D5CB58DD6D27Q51916654-C28BFDFF-BF82-4768-AD1B-864AD502C969Q51923447-C44B9376-1A0D-447D-A8E0-EB9D6C0F9606Q52329702-92D9546F-15EF-42C7-A1B0-107B06A5FE6DQ52746207-A357A8A4-EA5D-4B1B-B57F-9BA6C11F45BFQ52746212-A065F7E7-2AB2-4FF1-9806-89B1ACF0B452
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Marco Pierini
@ast
Marco Pierini
@en
Marco Pierini
@es
Marco Pierini
@nl
Marco Pierini
@sl
type
label
Marco Pierini
@ast
Marco Pierini
@en
Marco Pierini
@es
Marco Pierini
@nl
Marco Pierini
@sl
prefLabel
Marco Pierini
@ast
Marco Pierini
@en
Marco Pierini
@es
Marco Pierini
@nl
Marco Pierini
@sl
P106
P1153
10641355700
P21
P31
P496
0000-0003-4030-8205