%D8%AC%D9%88%D9%86_%D9%87%D8%A7%D8%B1%D8%AA%D9%81%D9%8A%D8%AC%D8%AC%D8%A7%D9%86_%D8%A7%D9%81._%D9%87%D8%A7%D8%B1%D8%AA%D9%88%DB%8C%D9%82Category:John_F._HartwigJohn_F._HartwigJohn_F._Hartwig%D8%AC%D8%A7%D9%86_%D8%A7%D9%81._%D9%87%D8%A7%D8%B1%D8%AA%D9%88%DB%8C%DA%AF%D0%A5%D0%B0%D1%80%D1%82%D0%B2%D0%B8%D0%B3,_%D0%94%D0%B6%D0%BE%D0%BDQ15432304
about
Undirected, Homogeneous C-H Bond Functionalization: Challenges and OpportunitiesInfluences on the Relative Rates for C−N Bond-Forming Reductive Elimination and β-Hydrogen Elimination of Amides. A Case Study on the Origins of Competing Reduction in the Palladium-Catalyzed Amination of Aryl HalidesPalladium-catalyzed formation of carbon-nitrogen bonds. Reaction intermediates and catalyst improvements in the hetero cross-coupling of aryl halides and tin amidesPalladium-Catalyzed α-Arylation of Carbonyl Compounds and NitrilesPalladium-Catalyzed Amination of Aryl Triflates and Importance of Triflate Addition RateEvolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl HalidesRuthenium-Catalyzed Regiospecific Borylation of Methyl C−H BondsA Rare, Low-Valent Alkylamido Complex, a Diphenylamido Complex, and Their Reductive Elimination of Amines by Three-Coordinate IntermediatesCarbon−Nitrogen-Bond-Forming Reductive Elimination of Arylamines from Palladium(II) Phosphine ComplexesPalladium-Catalyzed C−O Coupling Involving Unactivated Aryl Halides. Sterically Induced Reductive Elimination To Form the C−O Bond in Diaryl EthersCatalytic organometallic reactions of ammonia.Enantioselective alpha-arylation of ketones with aryl triflates catalyzed by difluorphos complexes of palladium and nickelFluorescence resonance energy transfer (FRET) as a high-throughput assay for coupling reactions. Arylation of amines as a case study.Palladium-catalyzed coupling of ammonia with aryl chlorides, bromides, iodides, and sulfonates: a general method for the preparation of primary arylamines.Beyond Iron: Iridium-Containing P450 Enzymes for Selective Cyclopropanations of Structurally Diverse Alkenes.Carbon-heteroatom bond formation catalysed by organometallic complexesIridium-catalyzed enantioselective allylic substitution of unstabilized enolates derived from α,β-unsaturated ketones.Highly reactive, single-component nickel catalyst precursor for Suzuki-Miyuara cross-coupling of heteroaryl boronic acids with heteroaryl halides.Selective C-H fluorination of pyridines and diazines inspired by a classic amination reaction.One-pot synthesis of unsymmetrical diaryl thioethers by palladium-catalyzed coupling of two aryl bromides and a thiol surrogate.Iridium-catalyzed regio- and enantioselective allylic substitution of silyl dienolates derived from dioxinonesCopper(I) phenoxide complexes in the etherification of aryl halides.Kumada coupling of aryl and vinyl tosylates under mild conditions.Direct measurement of the thermodynamics of vinylarene hydroamination.Direct, catalytic hydroaminoalkylation of unactivated olefins with N-alkyl arylaminesMetal-catalysed azidation of tertiary C-H bonds suitable for late-stage functionalizationRecent advances in the discovery of organometallic catalysts using high-throughput screening assays.Origins of Regioselectivity in Iridium Catalyzed Allylic Substitution.Synthesis of Copper(I) Thiolate Complexes in the Thioetherification of Aryl Halides.Electronic effects on reductive elimination to form carbon-carbon and carbon-heteroatom bonds from palladium(II) complexes.Hydroaminoalkylation of unactivated olefins with dialkylamines.Trifluoromethylation of Arylsilanes with [(phen)CuCF3 ]Late Stage Azidation of Complex Molecules.Palladium-Catalyzed, Site-Selective Direct Allylation of Aryl C-H Bonds by Silver-Mediated C-H Activation: A Synthetic and Mechanistic Investigation.Enantioselective functionalization of allylic C-H bonds following a strategy of functionalization and diversification.Editing the stereochemical elements in an iridium catalyst for enantioselective allylic amination.Iridium-Catalyzed Enantioselective Allylic Substitution of Enol Silanes from Vinylogous Esters and Amides.Cation control of diastereoselectivity in iridium-catalyzed allylic substitutions. Formation of enantioenriched tertiary alcohols and thioethers by allylation of 5H-oxazol-4-ones and 5H-thiazol-4-ones.Correction to "Copper-Mediated C-N Coupling of Arylsilanes with Nitrogen Nucleophiles".Regioselectivity of the borylation of alkanes and arenes.
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subject
description
Ameerika Ühendriikide keemik
@et
American chemist
@en
Amerikaans scheikundige
@nl
US-amerikanischer Chemiker
@de
Usana kemiisto
@io
ceimiceoir Meiriceánach
@ga
chimist american
@ro
chimiste américain
@fr
cimiciste american
@lfn
kiemavan Lamerikänik
@vo
name
John F. Hartwig
@ast
John F. Hartwig
@ca
John F. Hartwig
@de
John F. Hartwig
@en
John F. Hartwig
@es
John F. Hartwig
@fr
John F. Hartwig
@ga
John F. Hartwig
@nl
John F. Hartwig
@sl
Джон Хартвиг
@ru
type
label
John F. Hartwig
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John F. Hartwig
@ca
John F. Hartwig
@de
John F. Hartwig
@en
John F. Hartwig
@es
John F. Hartwig
@fr
John F. Hartwig
@ga
John F. Hartwig
@nl
John F. Hartwig
@sl
Джон Хартвиг
@ru
altLabel
ジョン・F・ハートウィッグ
@ja
prefLabel
John F. Hartwig
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John F. Hartwig
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John F. Hartwig
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John F. Hartwig
@en
John F. Hartwig
@es
John F. Hartwig
@fr
John F. Hartwig
@ga
John F. Hartwig
@nl
John F. Hartwig
@sl
Джон Хартвиг
@ru
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P1006
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P1006
P1343
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