about
An NMR and ab initio quantum chemical study of acid-base equilibria for conformationally constrained acidic alpha-amino acids in aqueous solution.Prediction of enantioselectivity in rhodium catalyzed hydrogenations.Investigating the nature of palladium chain-walking in the enantioselective redox-relay Heck reaction of alkenyl alcoholsStereoselectivity in Asymmetric Catalysis: The Case of Ruthenium-Catalyzed Ketone Hydrogenation.Prediction of Stereochemistry using Q2MM.Mechanism, reactivity, and selectivity in palladium-catalyzed redox-relay Heck arylations of alkenyl alcohols.Iron-catalyzed coupling of aryl Grignard reagents with alkyl halides: a competitive Hammett studyDevelopment of a Q2MM Force Field for the Asymmetric Rhodium Catalyzed Hydrogenation of Enamides.Breaking Conjugation: Unusual Regioselectivity with 2-Substituted Allylic Substrates in the Tsuji-Trost Reaction.Design and synthesis of a new type of ferrocene-based planar chiral DMAP analogues. A new catalyst system for asymmetric nucleophilic catalysis.Modeling the stereoselectivity of the beta-amino alcohol-promoted addition of dialkylzinc to aldehydes.Pd- η3 -C6H9 complexes of the Trost modular ligand: high nuclearity columnar aggregation controlled by concentration, solvent and counterion.Anomeric Effects in Sulfamides.On the radical nature of iron-catalyzed cross-coupling reactions.Structure-based rationale for selectivity in the asymmetric allylic alkylation of cycloalkenyl esters employing the Trost 'Standard Ligand' (TSL): isolation, analysis and alkylation of the monomeric form of the cationic eta(3)-cyclohexenyl complex [Competing Pathways in O-Arylations with Diaryliodonium Salts: Mechanistic Insights.Fast and reversible insertion of carbon dioxide into zirconocene-alkoxide bonds. A mechanistic study.Molecular modeling of bifunctional chelate peptide conjugates. 1. Copper and indium parameters for the AMBER force field.S-adenosylmethionine conformations in solution and in protein complexes: conformational influences of the sulfonium group.Investigation of the metal binding site in methionine aminopeptidase by density functional theory.Phenyl versus ethyl transfer in the addition of organozinc reagents to aldehydes: a theoretical study.Experimental and quantum-mechanical investigation of the vinylsilane-iminium ion cyclization.Structure investigation of TiIV-BODOLates involved in the catalytic asymmetric reduction of ketones using catecholborane.A dynamic supramolecular system exhibiting substrate selectivity in the catalytic epoxidation of olefins.Copper-catalyzed cross-couplings with part-per-million catalyst loadings.A new strategy for the improvement of photophysical properties in ruthenium(II) polypyridyl complexes. Synthesis and photophysical and electrochemical characterization of six mononuclear ruthenium(II) bisterpyridine-type complexes.On the nature of the intermediates and the role of chloride ions in Pd-catalyzed allylic alkylations: added insight from density functional theory.Combined experimental and theoretical study of the mechanism and enantioselectivity of palladium- catalyzed intermolecular Heck coupling.Me2Zn-mediated addition of acetylenes to aldehydes and ketones.Steric influence on the excited-state lifetimes of ruthenium complexes with bipyridyl-alkanylene-pyridyl ligands.Probing competitive enantioselective approach vectors operating in the Jacobsen-Katsuki epoxidation: a kinetic study of methyl-substituted styrenes.An experimental and theoretical study of the mechanism of stannylcupration of alpha,beta-acetylenic ketones and esters.Divergence en route to nonclassical annonaceous acetogenins. Synthesis of pyranicin and pyragonicin.Conformational Preference of 2-(Halomethyl)- and 2-(Oxymethyl)Pyridines: Microwave Spectrum, Ab Initio, and MM3 Studies of 2-(Fluoromethyl)Pyridine.Deconvoluting the memory effect in Pd-catalyzed allylic alkylation: Effect of leaving group and added chloride.Computational prediction of chemical reactions: current status and outlook.tBu or not tBu?Single-Flask Multicomponent Palladium-Catalyzed α,γ-Coupling of Ketone Enolates: Facile Preparation of Complex Carbon Scaffolds.Transition-State Docking of Flunitrazepam and Progesterone in Cytochrome P450.DFT investigation of the palladium-catalyzed ene-yne coupling.
P50
Q30656493-B7033714-D8A9-41AE-A2F9-4DE65AFB5439Q33399595-10C2EF23-0098-4FF8-B11A-4DFCEDEF20D9Q34764413-3EE6CBF6-9C72-454B-98C3-A073ECC456F5Q35845179-01EAD858-8244-4959-97AD-0A9365BA7574Q35985618-9972908C-3DDE-417B-9820-687D960B9D0FQ37701627-26FA651D-3A1B-48CE-AB4B-20624C566843Q39578032-66642452-B87A-4E4B-9CE2-5F07D6BE89C8Q40247800-4DBB8526-241E-48A6-8667-0422AAF28295Q40293448-3485FA4C-82AD-4D3B-8A5F-4A97C2026AD5Q40383168-8AEF47D7-B9BB-47DA-A6B6-EE1A6C72B36CQ40592423-7255E255-0A92-41F8-A2F0-FF3CCD929CEEQ41083107-144092CC-00A4-4A62-B2B0-921AF96EEDC0Q41240143-34871C41-0EFE-426A-9BCD-57FD868D82ACQ41374605-3F48051E-21A1-425B-B00B-DF53C8D00271Q42163089-1A7F78A5-7227-4533-B4A7-5CC7AE4D2F30Q42702395-E9E91FD5-B205-4AE3-8AF3-06AFC392EC48Q43539001-A81A6B1B-3435-4542-8AE1-3E2F3234D939Q43739036-7B0479B1-94E1-43FF-B79A-777101F2FCB9Q44022506-3263ACB2-0285-4226-BD7D-9C5BDA465414Q44167538-3408C30E-F686-47C6-A6FD-2B670DB7A4AFQ44507396-F2FACC83-3A16-414D-A530-D376B172B650Q44556886-3AAAEA95-1B34-483B-8762-65A0FD316AD4Q44706203-7936FE10-4FE8-469D-9760-0CB848E291DBQ45227121-50271D02-89D5-4822-A10B-3E5F9466BC16Q45953587-5EB587D7-6F00-4F49-8503-DB6778DF9224Q46451420-B72F2CEE-B72F-40D7-80B5-F1E97C803CE2Q46481320-0E5718F5-1C05-4AE2-A6E4-BBD569FFBB8DQ46488377-6E420A39-CD7F-4D35-B3E6-C3826088178FQ46576501-855ADC18-A3F2-4B52-8668-8BF62EC0F61CQ46652713-8B59C0C4-2F28-44F0-A6F3-42E48793D0B1Q46725591-058B8E48-ECB8-48FD-9EEF-FBF05FA0272AQ46902965-BB00F5D2-1C13-4CEE-A5D3-1FF59C61594EQ46959495-8711A2A8-1B48-4623-A329-3E7F6B60F8F9Q49603926-E0B6CD16-96E7-4046-A900-4D18FF812611Q51983011-C903DE0D-1516-4F8B-BB1C-EA2467C4EFA6Q52671641-4A635D6A-8223-47B1-8E7F-1389866DD5E7Q52732611-171838EB-6172-4973-B2F1-59F53DB255FFQ53579158-2DE4A41F-1854-4373-A511-A719C8C4A362Q54354672-A53AFB29-0721-4DC9-AFB0-7DCFE196C0E9Q54667698-C2406154-83B3-4950-8F87-C281D94ED761
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Per-Ola Norrby
@ast
Per-Ola Norrby
@en
Per-Ola Norrby
@es
Per-Ola Norrby
@nl
Per-Ola Norrby
@sl
type
label
Per-Ola Norrby
@ast
Per-Ola Norrby
@en
Per-Ola Norrby
@es
Per-Ola Norrby
@nl
Per-Ola Norrby
@sl
prefLabel
Per-Ola Norrby
@ast
Per-Ola Norrby
@en
Per-Ola Norrby
@es
Per-Ola Norrby
@nl
Per-Ola Norrby
@sl
P1053
A-3399-2009
P106
P31
P3829
P496
0000-0002-2419-0705