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Determination of absolute configuration of acyclic 1,2-diols with [Mo2(OAc)4], part 2: new structural evidence toward a rationale of the method: what remains of [Mo2(OAc)4] in DMSO solution?Studies on the interactions between some flavonols and cyclodextrins.Cyclodextrins as carriers for kavalactones in aqueous media: spectroscopic characterization of (S)-7,8-dihydrokavain and beta-cyclodextrin inclusion complex.Yeast frataxin is stabilized by low salt concentrations: cold denaturation disentangles ionic strength effects from specific interactions.New mono- and dimeric members of the secalonic acid family: blennolides A-G isolated from the fungus Blennoria sp.Glucose-coated superparamagnetic iron oxide nanoparticles prepared by metal vapour synthesis are electively internalized in a pancreatic adenocarcinoma cell line expressing GLUT1 transporter.Structural and chiroptical properties of the two coordination isomers of YbDOTA-type complexes.Elucidation of 1H NMR Paramagnetic Features of Heterotrimetallic Lanthanide(III)/Manganese(III) 12-MC-4 Complexes.Structure and absolute configuration of new diterpenes from Lavandula multifida.The "Case of Two Compounds with Similar Configuration but Nearly Mirror Image CD Spectra" Refuted. Reassignment of the Absolute Configuration of N-Formyl-3',4'-dihydrospiro[indan-1,2'(1'H)-pyridine].Presence of a putative steroidal allosteric site on glycoprotein hormone receptors.In situ assembly of octahedral Fe(II) complexes for the enantiomeric excess determination of chiral amines using circular dichroism spectroscopy.Axial Ligand exchange in chiral macrocyclic ytterbium(III) complexes.[Ln(binolam)3]·(OTf)3, a new class of propeller-shaped lanthanide(III) salt complexes as enantioselective catalysts: structure, dynamics and mechanistic insight.Systematic investigation of CD spectra of aryl benzyl sulfoxides interpreted by means of TDDFT calculations.Interactions between quercetin and warfarin for albumin binding: A new eye on food/drug interference.Xanthones and oxepino[2, 3-b]chromones from three endophytic fungi.Determination of absolute configuration of acyclic 1,2-diols with Mo2(OAc)4. 1. Snatzke's method revisited.Antioxidant principles from Bauhinia tarapotensis.Yb(fod)3 in the spectroscopic determination of the configuration of chiral diols: a survey of the lanthanide diketonate method.Assignment of absolute configuration of chiral carboxylic acids via exciton-coupled CD treatment: 4-phenylthioproline as a case study.Lanthanide circularly polarized luminescence: bases and applications.Absolute stereochemistry of dihydrofuroangelicins bearing C-8 substituted double bonds: a combined chemical/exciton chirality protocol.A TDDFT/MMPol/PCM model for the simulation of exciton-coupled circular dichroism spectra.Ligand lability and chirality inversion in yb heterobimetallic catalysts.Chirality driven self-assembly in a fluorescent organogel.A simple and general method to determine reliable pseudocontact shifts in lanthanide complexes.Stereochemical analysis of β-keto sulfoxides by circular dichroism.Circularly Polarized Luminescence of Silica-Grafted Europium Chiral Derivatives Prepared through a Sequential Functionalization.Strongly Circularly Polarized Emission from Water-Soluble Eu(III)- and Tb(III)-Based Complexes: A Structural and Spectroscopic Study.Absolute stereochemistry assignment of N-phosphorylimine-derived aza-Diels-Alder adducts with TDDFT CD calculations.Circular dichroism of tocopherols versus tocotrienols.The solution structure of a lasalocid A metal complex in lipophilic solvents.Optical Activity in the Near-IR Region: The λ=980 nm Multiplet of Chiral Yb(3+) Complexes.Circularly polarized luminescence under near-UV excitation and structural elucidation of a Eu complex.Enantiopure Cycloiridiated Complexes Bearing a Pentahelicenic N-Heterocyclic Carbene and Displaying Long-Lived Circularly Polarized Phosphorescence.Synthesis, Structural Characterization, and Chiroptical Studies of Bidentate Salen-Type Lanthanide (III) Complexes.Revision of the Absolute Configuration of Preussilides A-F Established by the Exciton Chirality Method.Exciton coupling between enones: Quassinoids revisited.Circularly Polarized Luminescence from Axially Chiral BODIPY DYEmers: An Experimental and Computational Study.
P50
Q30910700-096B1A16-B27A-4976-B1E9-7E1BD81C8E47Q31128123-ED47221E-874D-4AAB-A0C8-13A696C957CAQ33534561-21D25C7D-B2E7-4C9E-849A-70836E166CA9Q33572719-58D30F62-1C6B-49A0-AA58-0CF335BEB7E9Q34772116-8142B42F-563D-4D9D-88B1-C4ABF1F04EF0Q35432014-9DA7C380-43C3-419D-92D6-D23ED64C3B60Q37283913-A3A58A46-0706-4A2A-A3A5-8E56B680EE16Q38693275-9EDE7EE1-9612-48E3-8244-5DC1AE41E0A6Q39362255-EFE1378F-E544-4C2A-A12B-254446AE23B1Q39554811-7B21D0DA-329F-4DBB-969C-A78CEFC324EAQ39797568-BE79D131-2C47-420A-AB7A-57275BF071A2Q42540411-68124CFC-5D28-4B79-A3EC-AB5C0F3CE5B8Q42619922-86BCA86D-BC28-4634-80DB-A667852480A0Q42854686-73DA9600-2AEA-4905-B85F-1ECB7EA65E4DQ43184670-C7475B42-4284-4A33-B862-E08B842EF342Q43245062-5087A77F-29B5-4589-8E16-3875F6FCABBCQ43272166-8845A447-FC38-4AEF-958C-834542B1139EQ43665848-3B2EC5C5-5B91-4D40-8CDD-46F1714126A0Q43688138-6FF118AC-DDF2-4ADD-8E59-3F8FECE0A5CFQ43968159-3C6BBE72-0E2B-43D0-ABBE-A31F538AD08FQ44069061-54A9A3D7-66D0-41DF-93C9-75CF3C2C5180Q44397754-9A7E6A17-DD7C-4DA5-A267-EDCBAFE1133AQ44737905-5D89E5E2-AD82-40A8-B046-3DA67BA79940Q44755495-60B4FE66-E2CE-415B-929A-12309D4410A8Q45066333-7A0BA3EF-A6F6-476D-B0DA-1372981E0BFEQ45762640-FE101E8D-438E-4910-A643-41DD2A9E8C77Q46011409-5DAAFBA2-0F1C-4E8B-8760-D05CA19EC717Q46268297-66A9103A-738A-418E-8213-A46B878C163FQ46361212-E40D52B9-292E-4D06-903F-0FB6317DB43FQ46388139-19A1DCE5-68F6-473A-BF18-58B865009888Q46459672-93E55E8D-E5AE-4496-806E-E143EA2EEACBQ46534307-5D8F3AFE-725B-433E-8830-334B24CF8B50Q46579919-4A6D2D04-AF77-4DA4-85C1-18298C628EF7Q46694411-4388817B-AB01-4F94-A579-4ECEBC1D4EC5Q46709654-6ACEE9B7-CA05-4FBE-9A6D-F0458463B4B2Q48093349-C4ACB41A-8D74-4B77-B8A8-4BE635DE1486Q48126451-01DC97A3-CA58-41C0-86D7-4C3DC440D4ECQ48175564-0CF29DD8-DA41-41C3-B372-3ADCF480AA3DQ48247240-A67DD704-975A-4472-B9F0-B99ED9D34BA0Q48286839-608E4AA6-B495-4B0A-9A50-0B74C20A99CB
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Lorenzo Di Bari
@ast
Lorenzo Di Bari
@en
Lorenzo Di Bari
@es
Lorenzo Di Bari
@nl
Lorenzo Di Bari
@sl
type
label
Lorenzo Di Bari
@ast
Lorenzo Di Bari
@en
Lorenzo Di Bari
@es
Lorenzo Di Bari
@nl
Lorenzo Di Bari
@sl
prefLabel
Lorenzo Di Bari
@ast
Lorenzo Di Bari
@en
Lorenzo Di Bari
@es
Lorenzo Di Bari
@nl
Lorenzo Di Bari
@sl
P1053
H-4804-2015
P106
P1153
7003323257
P21
P31
P3829
P496
0000-0003-2347-2150