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Metal-ligand cooperation by aromatization-dearomatization as a tool in single bond activationReactivity studies of pincer bis-protic N-heterocyclic carbene complexes of platinum and palladium under basic conditionsA novel liquid organic hydrogen carrier system based on catalytic peptide formation and hydrogenation.Iridium-catalyzed asymmetric hydrogenation of racemic α-substituted lactones to chiral diols.CH2 Linkage Effects on the Reactivity of Bis(aminophosphine)-Ruthenium Complexes for Selective Hydrogenation of Esters into Alcohols.Neutral iridium catalysts with chiral phosphine-carboxy ligands for asymmetric hydrogenation of unsaturated carboxylic acids.New avenues for ligand-mediated processes--expanding metal reactivity by the use of redox-active catechol, o-aminophenol and o-phenylenediamine ligands.The contrasting catalytic efficiency and cancer cell antiproliferative activity of stereoselective organoruthenium transfer hydrogenation catalysts.The Development of Phosphine-Free "Tethered" Ruthenium(II) Catalysts for the Asymmetric Reduction of Ketones and Imines.Imino Transfer Hydrogenation Reductions.Easy To Synthesize, Robust Organo-osmium Asymmetric Transfer Hydrogenation Catalysts.Hydrogen-bonding pincer complexes with two protic N-heterocyclic carbenes from direct metalation of a 1,8-bis(imidazol-1-yl)carbazole by platinum, palladium, and nickel.Naked d-orbital in a centrochiral Ni(II) complex as a catalyst for asymmetric [3+2] cycloaddition.Selective hydrogen production from methanol with a defined iron pincer catalyst under mild conditions.Palladium-Catalysed Cross-Coupling Reactions Controlled by Noncovalent Zn⋅⋅⋅N Interactions.Comparative Study of Bifunctional Mononuclear and Dinuclear Amidoiridium Complexes with Chiral C-N Chelating Ligands for the Asymmetric Transfer Hydrogenation of Ketones.Facile synthesis and versatile reactivity of an unusual cyclometalated rhodium(I) pincer complex.Amine-free reversible hydrogen storage in formate salts catalyzed by ruthenium pincer complex without pH control or solvent change.CNN pincer ruthenium catalysts for hydrogenation and transfer hydrogenation of ketones: experimental and computational studies.Nickel-catalyzed asymmetric hydrogenation of β-acylamino nitroolefins: an efficient approach to chiral amines.Iridium Complexes with Proton-Responsive Azole-Type Ligands as Effective Catalysts for CO2 Hydrogenation.Differential Many-Body Cooperativity in Electronic Spectra of Oligonuclear Transition-Metal Complexes.Unsymmetrical Iron P-NH-P' Catalysts for the Asymmetric Pressure Hydrogenation of Aryl Ketones.Supported C-Scorpionate Vanadium(IV) Complexes as Reusable Catalysts for Xylene Oxidation.Asymmetric Hydrogenation of Vinylthioethers: Access to Optically Active 1,5-Benzothiazepine Derivatives.Molecularly Defined Manganese Pincer Complexes for Selective Transfer Hydrogenation of Ketones.Catalytic Enantioselective [3 + 2] Cycloaddition of α-Keto Ester Enolates and Nitrile Oxides.Efficient Palladium-Catalyzed Alkoxycarbonylation of Bulk Industrial Olefins Using Ferrocenyl Phosphine Ligands.Addition of H2 Across a Cobalt-Phosphorus Bond.Ruthenium PNN(O) Complexes: Cooperative Reactivity and Application as Catalysts for Acceptorless Dehydrogenative Coupling Reactions.Oxygen Evolution Catalyzed by a Mononuclear Ruthenium Complex Bearing Pendant SO3(-) Groups.Ruthenium complexes bearing an unsymmetrical pincer ligand with a 2-hydroxypyridylmethylene fragment: active catalysts for transfer hydrogenation of ketones.Ru-catalyzed asymmetric hydrogenation of δ-keto Weinreb amides: enantioselective synthesis of (+)-Centrolobine.Development of a novel secondary phosphine oxide-ruthenium(ii) catalyst and its application for carbonyl reduction.Enhanced Hydrogen Generation from Formic Acid by Half-Sandwich Iridium(III) Complexes with Metal/NH Bifunctionality: A Pronounced Switch from Transfer Hydrogenation.Lewis acid promoted ruthenium(II)-catalyzed etherifications by selective hydrogenation of carboxylic acids/esters.C3-symmetry Mo3S4 aminophosphino clusters combining three sources of stereogenicity: stereocontrol directed by hydrogen bond interactions and ligand configuration.Dehydrogenation of formic acid by Ir-bisMETAMORPhos complexes: experimental and computational insight into the role of a cooperative ligand.Homo- and Heterodinuclear Ir and Rh Imine-functionalized Protic NHC Complexes: Synthetic, Structural Studies, and Tautomerization/Metallotropism Insights.Unsymmetrical pincer-type ruthenium complex containing β-protic pyrazole and N-heterocyclic carbene arms: comparison of Brønsted acidity of NH groups in second coordination sphere.
P2860
Q26859113-F8E000A3-969C-4DA3-8AAA-FD257C9C169BQ28830741-CFC1AE38-F3FA-4A65-B947-F20083370470Q30643702-7BC9F325-2979-444C-B0A3-758117642630Q33578946-C89C9475-F8FA-4B53-9B4B-3058E032D226Q33822396-839D1AAA-A2FB-4A3B-A317-29C1B9EB375DQ37741842-1EC048B3-1F96-47AD-81E4-66978B1E0FF8Q38543236-2DB27DD7-163D-4786-AC22-1A666F7B6C68Q38775808-A74C77FE-924E-40D9-B9DA-F0CB8B3C5CE3Q38927774-201BE7D4-E1B6-4348-BA4D-97B4865EBB04Q38940186-BDBA48CA-5A90-46F1-9845-BB5D6334A021Q40214217-F30D7723-5BA3-4C82-A51F-75FF21325D44Q40776357-44DD556D-5F17-447D-95E2-487486542BB9Q41957248-F429DC9D-4347-4F54-B71F-AC732069E273Q45798212-9198D716-83EB-4B72-AD10-45328496AF0DQ46437182-5948BC20-8B42-41D9-9215-9B869553CAA3Q46476059-5D5EB6F2-B6EE-4827-AB06-682D6FF8284CQ46753675-79BEAF36-D18E-4B43-B9AD-43A9ABA09297Q46797607-FBFA5A10-E59F-40E5-BE44-1CB4D1C8CD61Q46842318-53BF4D35-B744-46CD-81D7-5F1ED3F92440Q47128637-78C7CF3C-2143-499F-BFB1-FDBD6E7565E2Q47854673-A71B7CA4-DCFC-42DC-8228-B969BCF82971Q48045018-15055ED1-7B09-4CDD-AEEA-66A381972045Q48096675-04D7EF77-6861-4493-914E-B6A02677E988Q48182455-389B18CC-F1CC-4B65-9B9C-706414D3D809Q48246490-01B29B21-D30A-460A-91D9-A2414D36E702Q48267725-BD24FC6E-3864-463F-B1DD-4F1D7EFF1FAEQ48327554-BE12E934-878F-4259-A7BE-FD7643084319Q48330202-CEFBD327-1FB2-42E7-A9AC-B316A5FB8C65Q48341842-F39623AB-1E7B-4940-B36B-909688ED6B5DQ49315798-3EA20CB2-3D10-484E-B504-E2CA0A524951Q50972169-42D929B8-3F41-486E-BA7A-3C1B02CC76C1Q51528495-6BC31914-5B85-4081-A9D5-EA2968D866BDQ51538173-88F45CFA-99DB-4223-959B-2CC0EF2008EFQ51770494-C7E99B86-8CE4-46D6-A787-97F2F1A17F49Q51807513-0D4ACD60-E49B-4948-B731-89923CF73F8AQ52794076-7EFEF73C-AAC4-4671-86AB-4A1C48F3D6E0Q53150485-FF1897F4-30AA-455A-8B80-6ED903C1D9C5Q53237780-8AAE456A-79E6-4B92-BA8B-1D25D908C88DQ53315708-3D289A9B-5501-4E20-8F5B-99ED83E59923Q53517342-8079744E-8517-4E5F-A76E-BE551316FE92
P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
The N-H functional group in organometallic catalysis.
@en
type
label
The N-H functional group in organometallic catalysis.
@en
prefLabel
The N-H functional group in organometallic catalysis.
@en
P2860
P356
P1476
The N-H functional group in organometallic catalysis
@en
P2093
Baoguo Zhao
Zhaobin Han
P2860
P304
P356
10.1002/ANIE.201204921
P407
P50
P577
2013-03-07T00:00:00Z