about
mRNA decapping is promoted by an RNA-binding channel in Dcp2Identification of efficient and sequence specific bimolecular artificial ribonucleases by a combinatorial approach.Atom-efficient gold(I)-chloride-catalyzed synthesis of α-sulfenylated carbonyl compounds from propargylic alcohols and aryl thiols: substrate scope and experimental and theoretical mechanistic investigation.Phosphine-catalyzed enantioselective intramolecular [3+2] annulations to generate fused ring systems.Phosphine-Catalyzed Doubly Stereoconvergent γ-Additions of Racemic Heterocycles to Racemic Allenoates: The Catalytic Enantioselective Synthesis of Protected α,α-Disubstituted α-Amino Acid Derivatives.Differential inhibition of mRNA degradation pathways by novel cap analogs.Mechanism and Selectivity of Cooperatively Catalyzed Meyer-Schuster Rearrangement/Tsuji-Trost Allylic Substitution. Evaluation of Synergistic Catalysis by Means of Combined DFT and Kinetics Simulations.Caution in the Use of Nonlinear Effects as a Mechanistic Tool for Catalytic Enantioconvergent Reactions: Intrinsic Negative Nonlinear Effects in the Absence of Higher-Order Species.Mechanism, reactivity, and selectivity of the iridium-catalyzed C(sp3)-H borylation of chlorosilanes.Novel dinucleoside 5',5'-triphosphate cap analogues. Synthesis and affinity for murine translation factor eIF4E.Kinetics of C. elegans DcpS cap hydrolysis studied by fluorescence spectroscopy.Mechanistic Insight into Enantioselective Palladium-Catalyzed Oxidative Carbocyclization-Borylation of Enallenes.N-Heterocyclic Carbene-Catalyzed Olefination of Aldehydes with Vinyliodonium Salts To Generate α,β-Unsaturated Ketones.Elucidation of Mechanisms and Selectivities of Metal-Catalyzed Reactions using Quantum Chemical Methodology.Effective Modulation of DNA Duplex Stability by Reversible Transition Metal Complex Formation in the Minor GrooveMechanism and Selectivity of Rhodium-Catalyzed 1:2 Coupling of Aldehydes and AllenesComputational Study of the Mechanism and Selectivity of Palladium-Catalyzed Propargylic Substitution with Phosphorus NucleophilesNovel, Stereoselective and Stereospecific Synthesis of Allenylphosphonates and Related Compounds via Palladium-Catalyzed Propargylic SubstitutionEfficient synthesis of mono- and diarylphosphinic acids: a microwave-assisted palladium-catalyzed cross-coupling of aryl halides with phosphinateA New Reagent System for Efficient Silylation of Alcohols: Silyl Chloride-N-Methylimidazole-IodinePd(0)-Catalyzed Phosphorus−Carbon Bond Formation. Mechanistic and Synthetic Studies on the Role of the Palladium Sources and Anionic AdditivesThe Case for the Intermediacy of Monomeric Metaphosphate Analogues during Oxidation ofH-Phosphonothioate,H-Phosphonodithioate, andH-Phosphonoselenoate Monoesters: Mechanistic and Synthetic StudiesOrganocatalytic Group Transfer Reactions with Hypervalent Iodine ReagentsCombining Meyer–Schuster Rearrangement with Aldol and Mannich Reactions: Theoretical Study of the Intermediate Interception Strategy31P NMR and Computational Studies on Stereochemistry of Conversion of Phosphoramidate Diesters into the Corresponding PhosphotriestersPreparation of benzylphosphonates via a palladium(0)-catalyzed cross-coupling of H-phosphonate diesters with benzyl halides. Synthetic and mechanistic studiesOn the Sulfurization ofH-Phosphonate Diesters and Phosphite Triesters Using Elemental SulfurPreparation of Arylphosphonates by Palladium(0)-Catalyzed Cross-Coupling in the Presence of Acetate Additives: Synthetic and Mechanistic StudiesIodine-promoted silylation of alcohols with silyl chlorides. Synthetic and mechanistic studiesMicrowave-Assisted Palladium-Catalyzed Cross-Coupling of Aryl and Vinyl Halides with H-Phosphonate DiestersPalladium-Catalyzed C−P Bond Formation: Mechanistic Studies on the Ligand Substitution and the Reductive Elimination. An Intramolecular Catalysis by the Acetate Group in PdIIComplexesSynthesis of nucleoside phosphorothio-, phosphorodithio- and phosphoroselenoate diesters via oxidative esterification of the corresponding H-phosphonate analoguesInteraction of human decapping scavenger with 5′ mRNA cap analogues: structural requirements for catalytic activityEnzymatically stable 5′ mRNA cap analogs: Synthesis and binding studies with human DcpS decapping enzymeA direct method for the synthesis of nucleoside 5′-methylenebis(phosphonate)s from nucleosidesSYNTHESIS AND BIOCHEMICAL PROPERTIES OF NOVEL mRNA 5′ CAP ANALOGS RESISTANT TO ENZYMATIC HYDROLYSISPalladium-catalyzed propargylic substitution with phosphorus nucleophiles: efficient, stereoselective synthesis of allenylphosphonates and related compoundsTransition-Metal-Free Aryl-Aryl Cross-Coupling: C-H Arylation of 2-Naphthols with Diaryliodonium Salts
P50
Q27649871-25E78429-EC02-451F-ACA6-A7371364E143Q33334539-2C8C9439-79EB-4D61-ACF9-B3968B1814DDQ35052259-CDDCAA9C-CCAE-4099-ABF9-5AAF8237F7C2Q35610293-42EAD4FC-5F54-40A4-84F8-FFFA721EC652Q36081059-53C4978D-71E9-4F89-BE6B-E2FD0C996874Q38319346-A76F025F-5CAC-4FF2-B28D-135500600A35Q38694451-158B4B25-4CBF-465C-A386-91795B564614Q38918773-9F9309BC-FA9D-4254-95F9-5BACE2B7610DQ43977854-421FE579-18F6-4DC8-9F41-12016ED493A8Q46773234-47866618-F88B-469B-B8C5-9297EADC5BB7Q46860837-6EABC8C7-A5E5-4CAD-A38E-AFF26571B731Q48368190-AC03138E-E05A-4938-81B8-1495AA22B137Q52656407-AC7F7C32-7CA9-446B-A871-59309E62ACADQ53139361-8081E1D2-EB56-4511-B63D-DFCA96BF0EE4Q59005628-D45CBFF0-47AF-48BA-837D-A97ED448EF84Q59255936-73E5B111-A926-4C9A-94D3-DB5C217C40A7Q59667064-705A336A-D33B-4202-A0CC-2C11F81EEB9AQ59667085-79CC1BDC-89D5-4B73-9734-1933958F0182Q59667134-B878DF24-4458-46E2-B1F4-E8DAE3AD95C8Q59667141-2665FB4D-B6D0-44AF-82D8-95FAC7D84160Q59667151-C38A0BA9-398D-4AE9-B27C-8EDA3B3275EBQ59667170-5CEEA808-337A-4BC4-9DE0-5C711DC87D0CQ59897825-425DE352-B538-4C96-AF9A-C4B10A8B5E07Q59897869-650E4010-F6B3-4FE2-8278-EF25A01E68B9Q59897888-99D951C5-43EE-44E0-A4C6-69C6D1A28076Q59897899-78DCDDFC-C639-4DBB-9C1B-9F907734A960Q59897910-41986BDB-3E02-49FF-B386-163F31026A7DQ59897919-18A37CBD-8D07-4CB9-B1B3-1E81726AD714Q59897937-F3D073A3-E60B-466F-91E3-E4EC6DD1D297Q59897943-1A588614-E30F-48FF-8B91-1390922FF389Q59897952-77A9D946-79A9-4421-8779-BAFB3D5D328AQ59897961-1B499C7A-F917-4C2F-8488-41DEC58DE689Q59897987-04DFBF26-7767-4384-B153-8227AD923A02Q59898011-1225DD9C-EEBA-4D62-AD28-9652610692C2Q59898020-07EBFB29-2CD5-4019-BC93-9C51A984F3B8Q59898033-3C1158EF-A838-4712-B782-FCC2F9E08539Q85053827-0A8A7B63-81FA-4CEB-A48D-907C80D719A2Q92513954-E41E29EF-3BE3-4E3A-AF9F-915707A0021C
P50
description
Polish researcher
@en
Pools onderzoeker
@nl
cercetător polonez
@ro
chercheur polonais
@fr
investigador polaco
@es
investigador polaco
@gl
investigador polonès
@ca
polnischer Forscher
@de
polski naukowiec
@pl
ricercatore polacco
@it
name
Marcin Kalek
@ast
Marcin Kalek
@es
Marcin Kalek
@nl
Marcin Kalek
@sl
Marcin Kałek
@ca
Marcin Kałek
@de
Marcin Kałek
@en
Marcin Kałek
@fr
Marcin Kałek
@ga
Marcin Kałek
@gl
type
label
Marcin Kalek
@ast
Marcin Kalek
@es
Marcin Kalek
@nl
Marcin Kalek
@sl
Marcin Kałek
@ca
Marcin Kałek
@de
Marcin Kałek
@en
Marcin Kałek
@fr
Marcin Kałek
@ga
Marcin Kałek
@gl
altLabel
Marcin Kalek
@en
prefLabel
Marcin Kalek
@ast
Marcin Kalek
@es
Marcin Kalek
@nl
Marcin Kalek
@sl
Marcin Kałek
@ca
Marcin Kałek
@de
Marcin Kałek
@en
Marcin Kałek
@fr
Marcin Kałek
@ga
Marcin Kałek
@gl
P108
P214
P5587
P906
P1053
B-6298-2013
P106
P1153
23027533100
P1412
P1559
Marcin Kałek
@pl
P21
P214
P27
P31
P3124
P3829
P496
0000-0002-1595-9818
P5587
qn25b0l82tn40fm
P569
1983-05-17T00:00:00Z
P735
P7859
viaf-171181705