about
Combined experimental and theoretical study on the reductive cleavage of inert C-O bonds with silanes: ruling out a classical Ni(0)/Ni(II) catalytic couple and evidence for Ni(I) intermediates.Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands.Catalytic intermolecular dicarbofunctionalization of styrenes with CO2 and radical precursors.An improved protocol for the Pd-catalyzed alpha-arylation of aldehydes with aryl halides.Metal-catalyzed activation of ethers via C-O bond cleavage: a new strategy for molecular diversity.Ni- and Fe-catalyzed Carboxylation of Unsaturated Hydrocarbons with CO2.Metal-catalyzed reductive coupling reactions of organic halides with carbonyl-type compounds.Pd-catalyzed intramolecular acylation of aryl bromides via C-H functionalization: a highly efficient synthesis of benzocyclobutenones.Ring-closing metathesis of chiral allylamines. Enantioselective synthesis of (2S,3R,4S)-3,4-dihydroxyproline.General approach to glycosidase inhibitors. Enantioselective synthesis of deoxymannojirimycin and swainsonine.A Mild and Ligand-Free Ni-Catalyzed Silylation via C-OMe Cleavage.Preparation, structure, and reactivity of nonstabilized organoiron compounds. Implications for iron-catalyzed cross coupling reactions.Cycloisomerization of enynes catalyzed by iron(0)-ate complexes.Ni-Catalyzed Regioselective Hydrocarboxylation of Alkynes with CO2 by Using Simple Alcohols as Proton Sources.A cheap metal for a "noble" task: preparative and mechanistic aspects of cycloisomerization and cycloaddition reactions catalyzed by low-valent iron complexes.Ni-catalyzed carboxylation of C(sp2)- and C(sp3)-O bonds with CO2.Site-Selective Catalytic Carboxylation of Unsaturated Hydrocarbons with CO2 and Water.Ni-Catalyzed Site-Selective Dicarboxylation of 1,3-Dienes with CO2.Nickel-Catalyzed Reductive Amidation of Unactivated Alkyl Bromides.Forging C-C Bonds Through Decarbonylation of Aryl Ketones.Switchable Site-Selective Catalytic Carboxylation of Allylic Alcohols with CO2.Visible-Light-Driven Carboxylation of Aryl Halides by the Combined Use of Palladium and Photoredox Catalysts.Ni-Catalyzed Stannylation of Aryl Esters via C-O Bond Cleavage.Ni-catalyzed Umpolung Arylation of Ambiphilic a-Bromo Boronic Esters.Walking Metals for Remote Functionalization.Ni-Catalyzed Borylation of Aryl Fluorides via C-F Cleavage.Nickel-Catalyzed Chemo-, Regio- and Diastereoselective Bond Formation through Proximal C-C Cleavage of Benzocyclobutenones.Ipso-Borylation of Aryl Ethers via Ni-Catalyzed C-OMe Cleavage.Nickel-catalyzed enantioselective C-C bond formation through C(sp2)-O cleavage in aryl esters.Ni-catalyzed direct reductive amidation via C-O bond cleavage.Ni-catalyzed reduction of inert C-O bonds: a new strategy for using aryl ethers as easily removable directing groups.A concise enantioselective entry to the synthesis of deoxy-azasugars.Cu-Catalyzed Tandem C−N Bond Formation for the Synthesis of Pyrroles and HeteroarylpyrrolesPd-Catalyzed Kumada−Corriu Cross-Coupling Reactions at Low Temperatures Allow the Use of Knochel-type Grignard ReagentsSite-Selective Ni-Catalyzed Reductive Coupling of α-Haloboranes with Unactivated OlefinsLigand-Controlled Regiodivergent Ni-Catalyzed Reductive Carboxylation of Allyl Esters with CO2Ni-Catalyzed Stereoselective Arylation of Inert C–O bonds at Low TemperaturesNickel-Catalyzed Decarbonylative CH Coupling Reactions: A Strategy for Preparing Bis(heteroaryl) BackbonesStereoselective Synthesis of 2-Acetamido-1,2-dideoxyallonojirimycin (DAJNAc), a New Potent Hexosaminidase InhibitorForging Amides Through Metal-Catalyzed C-C Coupling with Isocyanates
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Ruben Martin
@ast
Ruben Martin
@en
Ruben Martin
@es
Ruben Martin
@nl
Ruben Martin
@sl
type
label
Ruben Martin
@ast
Ruben Martin
@en
Ruben Martin
@es
Ruben Martin
@nl
Ruben Martin
@sl
prefLabel
Ruben Martin
@ast
Ruben Martin
@en
Ruben Martin
@es
Ruben Martin
@nl
Ruben Martin
@sl
P108
P1053
M-2905-2014
P106
P108
P21
P31
P3829
P496
0000-0002-2543-0221