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Denaturation of proteins by surfactants studied by the Taylor dispersion analysis.Synthesis and comprehensive structural and physicochemical characterization of dutasteride hydrochloride hydrate solvates.Enantioselective Extraction System Containing Binary Chiral Selectors and Chromatographic Enantioseparation Method for Determination of the Absolute Configuration of Enantiomers of CyclopentolateInduced circularly polarized luminescence for revealing DNA binding with fluorescent dyes.Glucosylceramide mimics: highly potent GCase inhibitors and selective pharmacological chaperones for mutations associated with types 1 and 2 Gaucher disease.Comprehensive spectroscopic characterization of finasteride polymorphic forms. Does the form X exist?Stereochemical analysis of β-keto sulfoxides by circular dichroism.Dimolybdenum tetracarboxylates as auxiliary chromophores in chiroptical studies of vic-diols.Synthesis and structure analysis of ferrocene-containing pseudopeptides.Chirality sensing of bioactive compounds with amino alcohol unit via circular dichroism.Pyriculins A and B, two monosubstituted hex-4-ene-2,3-diols and other phytotoxic metabolites produced by Pyricularia grisea isolated from buffelgrass (Cenchrus ciliaris).Polyoxygenated cyathane diterpenoids from the mushroom Cyathus africanus, and their neurotrophic and anti-neuroinflammatory activities.Syntheses, structures, and chiroptical and magnetic properties of chiral clusters built from Schiff bases: a novel [MnIIMnNa] core.Absolute Configuration Determination by Quantum Mechanical Calculation of Chiroptical Spectra: Basics and Applications to Fungal Metabolites.Phytotoxic Metabolites Produced by Diaporthella cryptica, the Causal Agent of Hazelnut Branch CankerColletopyrandione, a new phytotoxic tetrasubstituted indolylidenepyra n -2,4-dione, and colletochlorins G and H, new tetrasubstituted chroman- and isochroman-3,5-diols isolated from Colletotrichum higginsianumA configurational and conformational study of (-)-Oseltamivir using a multi-chiroptical approachComprehensive chiroptical study of proline-containing diamide compoundsCombined reversible switching of ECD and quenching of CPL with chiral fluorescent macrocyclesPhytotoxic Activity of Metabolites Isolated from , the Causal Agent of Bleach Blonde Syndrome on Cheatgrass ()Symmetry-Dependent Vibrational Circular Dichroism Enhancement in Co(II) Salicylaldiminato ComplexesEnantiopure C1-Cyclotriveratrylene with a Reversed Spatial Arrangement of the SubstituentsChiroptical methods in a wide wavelength range for obtaining Ln3+ complexes with circularly polarized luminescence of practical interestOn the Absolute Stereochemistry of Tolterodine: A Circular Dichroism StudyPractical method for the absolute configuration assignment of tert/tert 1,2-diols using their complexes with Mo2(OAc)4Distinguishing between polymorphic forms of linezolid by solid-phase electronic and vibrational circular dichroismTransmission vs. Diffuse Transmission in Circular Dichroism: What to Choose for Probing Solid-State Samples?Photoinduced isomerization of 23-oxosapogenins: conformational analysis and spectroscopic characterization of 22-isosapogeninsChromane helicity rule--scope and challenges based on an ECD study of various trolox derivativesAmine-catalyzed direct aldol reactions of hydroxy- and dihydroxyacetone: biomimetic synthesis of carbohydratesIn Depth Analysis of Chiroptical Properties of Enones Derived from Abietic AcidSynthesis and Comprehensive Structural and Chiroptical Characterization of Enones Derived from (-)-α-Santonin by Experiment and TheoryA Critical Appraisal of Dimolybdenum Tetraacetate Application in Stereochemical Studies of vic-Diols by Circular DichroismHigginsianins D and E, Cytotoxic Diterpenoids Produced by Colletotrichum higginsianumSolvation of 2-(hydroxymethyl)-2,5,7,8-tetramethyl-chroman-6-ol revealed by circular dichroism: a case of chromane helicity rule breakingUnique Aggregation of Sterigmatocystin in Water Yields Strong and Specific Circular Dichroism Response Allowing Highly Sensitive and Selective Monitoring of Bio-Relevant InteractionsChiral [MnII MnIII 3 M'] (M'=NaI , CaII , MnII ) and [MnII MnIII 6 NaI 2 ] Clusters Built from an Enantiomerically Pure Schiff Base: Synthetic, Chiroptical, and Magnetic PropertiesElusive π-helical peptide foldamers spotted by chiroptical studiesHelicene Monomers and Dimers: Chiral Chromophores Featuring Strong Circularly Polarized LuminescencePhytotoxic Metabolites from Three Neofusicoccum Species Causal Agents of Botryosphaeria Dieback in Australia, Luteopyroxin, Neoanthraquinone, and Luteoxepinone, a Disubstituted Furo-α-pyrone, a Hexasubstituted Anthraquinone, and a Trisubstituted Oxe
P50
Q33584799-AFE23AC3-F828-4978-A76C-5B4C2744C0F8Q36397806-ACE6F61A-744E-4272-844C-88E2F24ABF74Q37333946-5564C44A-6877-4F10-8A4C-3FB104E872CCQ38949609-D183468D-0999-4DBB-AD08-329516BB574FQ39081905-32223CAC-4201-492F-88CF-6F3BA96E5507Q41484045-3EF7795C-EDDC-4B1B-8444-3CFE0EB6DBDCQ46268297-29679A1D-6164-44AC-A72B-F95494246539Q46324038-F1CA4C0E-4E97-44D9-9F04-D1ED64E2F759Q48147716-EA58B140-AE99-4F81-9ED7-4CCC0913792DQ48297250-AF6FBA8F-45DD-4F57-A32D-F63222AC2216Q48354221-C68D4C37-3097-44A1-AF89-A1F5152559CBQ49389077-20F6F1E2-EF12-42FF-89AF-38559A923394Q53345388-AE03AE52-469D-412C-8E7B-4A14F37EA63CQ53795226-A708A987-8F78-40FC-9597-188C4FC7BBA3Q56787612-6E2E8270-7FE6-4301-BC5D-BC88AA2E0AD7Q56787665-27DDDE3A-537D-4884-8ECF-9F9E99A724B4Q57160538-E77DBCB4-4E37-46BC-ABC7-279CA9F162D9Q57164398-2171D922-3797-452F-AEDD-7D3E3073479EQ57495780-F7735A8C-E942-4605-B205-FCDBAC2D1467Q60173695-FF625C28-3A6E-4388-9F59-A164866842F0Q62261656-BF3FE5C5-B110-4395-8062-AF5FF9DB3D39Q62261663-C72DD516-5103-43C8-A740-9C98803EC2B0Q62261730-5C4AAA4D-A265-4231-97CB-829C54778056Q64230457-10593DC3-AE65-431B-A0B0-D5CFA98EF0AFQ80001913-8FD6051C-437A-4871-9445-F8A8FA15CDCDQ83704917-E55E7E79-A2B0-40E6-A362-8D5F8098C1EFQ85288343-9303F3C7-A044-4679-B871-6EE9EFBB8FF2Q85560593-6F9F8CA6-8E25-42D3-8E6E-37F14D47C91DQ87358490-2821A46E-2549-452D-A31E-97D66173418DQ87897433-A31DA3F5-FFE8-43D8-98F2-3C1E8B5B6B72Q87910672-BD8FA3EC-DF55-4625-815A-C798C3FA3FECQ89298539-7A27A1A9-2F98-4BFE-BA85-2C087458928BQ90142884-3F312CB8-F059-4BF9-81CC-EA058A4E4B81Q90456792-6DCC23A7-8A01-44CC-ACDD-2A78E13B0A68Q91119003-B71FD14A-94BE-461A-AD02-29B375EA57A7Q91168322-565EE6C2-5E9C-4C86-B070-E0EC422C0F8AQ91533255-6D237515-B25C-4FA6-AFDD-999E2BA48F8BQ92038050-EE15FDEB-FAED-41C9-9E96-DE4F149C7465Q92151521-01F5CFC7-810B-406B-B121-9BE80074EF13Q92725893-5D91B54E-CF33-4A75-B469-791799D539D4
P50
description
hulumtues
@sq
researcher
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wetenschapper
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հետազոտող
@hy
name
Marcin Górecki
@ast
Marcin Górecki
@en
Marcin Górecki
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Marcin Górecki
@nl
Marcin Górecki
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type
label
Marcin Górecki
@ast
Marcin Górecki
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Marcin Górecki
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Marcin Górecki
@nl
Marcin Górecki
@sl
prefLabel
Marcin Górecki
@ast
Marcin Górecki
@en
Marcin Górecki
@es
Marcin Górecki
@nl
Marcin Górecki
@sl
P106
P1153
36939918500
P21
P31
P496
0000-0001-7472-3875
P569
2000-01-01T00:00:00Z