Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Buchwald–Hartwig_amination> ?p ?o }
- Buchwald–Hartwig_amination abstract "The Buchwald–Hartwig amination is a chemical reaction used in organic chemistry for the synthesis of carbon–nitrogen bonds via the palladium-catalyzed cross-coupling of amines with aryl halides. Although Pd-catalyzed C-N couplings were reported as early as 1983, credit for its development is typically assigned to Stephen L. Buchwald and John F. Hartwig, whose publications between 1994 and the late 2000s established the scope of the transformation. The reaction's synthetic utility stems primarily from the shortcomings of typical methods (nucleophilic substitution, reductive amination, etc.) for the synthesis of aromatic C–N bonds, with most methods suffering from limited substrate scope and functional group tolerance. The development of the Buchwald–Hartwig reaction allowed for the facile synthesis of aryl amines, replacing to an extent harsher methods (the Goldberg reaction, nucleophilic aromatic substitution, etc.) while significantly expanding the repertoire of possible C–N bond formation.Over the course of its development, several 'generations' of catalyst systems have been developed, with each system allowing greater scope in terms of coupling partners and milder conditions, allowing virtually any amine to be coupled with a wide variety of aryl coupling partners. Because of the ubiquity of aryl C-N bonds in pharmaceuticals and natural products, the reaction has gained wide use in synthetic organic chemistry, finding application in many total syntheses and the industrial preparation of numerous pharmaceuticals. Several reviews have been published.".
- Buchwald–Hartwig_amination thumbnail Buchwaldhartwig.png?width=300.
- Buchwald–Hartwig_amination wikiPageExternalLink buchwald-hartwig-reaction.shtm.
- Buchwald–Hartwig_amination wikiPageExternalLink powerpoint-ian-buchhart.pdf.
- Buchwald–Hartwig_amination wikiPageExternalLink search=%22Buchwald-Hartwig%20reaction%22.
- Buchwald–Hartwig_amination wikiPageExternalLink buchwald-hartwig-amination.
- Buchwald–Hartwig_amination wikiPageID "6691097".
- Buchwald–Hartwig_amination wikiPageLength "28867".
- Buchwald–Hartwig_amination wikiPageOutDegree "90".
- Buchwald–Hartwig_amination wikiPageRevisionID "682821402".
- Buchwald–Hartwig_amination wikiPageWikiLink 1,1-Bis(diphenylphosphino)ferrocene.
- Buchwald–Hartwig_amination wikiPageWikiLink Alcohol.
- Buchwald–Hartwig_amination wikiPageWikiLink Amine.
- Buchwald–Hartwig_amination wikiPageWikiLink Ammonia.
- Buchwald–Hartwig_amination wikiPageWikiLink Aniline.
- Buchwald–Hartwig_amination wikiPageWikiLink Arene_substitution_pattern.
- Buchwald–Hartwig_amination wikiPageWikiLink Argon.
- Buchwald–Hartwig_amination wikiPageWikiLink Atomic_orbital.
- Buchwald–Hartwig_amination wikiPageWikiLink BINAP.
- Buchwald–Hartwig_amination wikiPageWikiLink Base_(chemistry).
- Buchwald–Hartwig_amination wikiPageWikiLink Benzophenone.
- Buchwald–Hartwig_amination wikiPageWikiLink Beta-Hydride_elimination.
- Buchwald–Hartwig_amination wikiPageWikiLink Biphenyl.
- Buchwald–Hartwig_amination wikiPageWikiLink Bite_angle.
- Buchwald–Hartwig_amination wikiPageWikiLink Buchwald–Hartwig_amination.
- Buchwald–Hartwig_amination wikiPageWikiLink Carbonate.
- Buchwald–Hartwig_amination wikiPageWikiLink Carbon–nitrogen_bond.
- Buchwald–Hartwig_amination wikiPageWikiLink Catalysis.
- Buchwald–Hartwig_amination wikiPageWikiLink Category:Name_reactions.
- Buchwald–Hartwig_amination wikiPageWikiLink Category:Substitution_reactions.
- Buchwald–Hartwig_amination wikiPageWikiLink Chelation.
- Buchwald–Hartwig_amination wikiPageWikiLink Chemical_equilibrium.
- Buchwald–Hartwig_amination wikiPageWikiLink Chemical_reaction.
- Buchwald–Hartwig_amination wikiPageWikiLink Chloride.
- Buchwald–Hartwig_amination wikiPageWikiLink Copper.
- Buchwald–Hartwig_amination wikiPageWikiLink Dale_L._Boger.
- Buchwald–Hartwig_amination wikiPageWikiLink Denticity.
- Buchwald–Hartwig_amination wikiPageWikiLink Diethylamine.
- Buchwald–Hartwig_amination wikiPageWikiLink Ether.
- Buchwald–Hartwig_amination wikiPageWikiLink Ferrocene.
- Buchwald–Hartwig_amination wikiPageWikiLink Hydroxide.
- Buchwald–Hartwig_amination wikiPageWikiLink Imine.
- Buchwald–Hartwig_amination wikiPageWikiLink Intermolecular_force.
- Buchwald–Hartwig_amination wikiPageWikiLink Intramolecular_reaction.
- Buchwald–Hartwig_amination wikiPageWikiLink Iodide.
- Buchwald–Hartwig_amination wikiPageWikiLink John_F._Hartwig.
- Buchwald–Hartwig_amination wikiPageWikiLink Journal_of_the_American_Chemical_Society.
- Buchwald–Hartwig_amination wikiPageWikiLink Ligand.
- Buchwald–Hartwig_amination wikiPageWikiLink Lithium_bis(trimethylsilyl)amide.
- Buchwald–Hartwig_amination wikiPageWikiLink Natural_product.
- Buchwald–Hartwig_amination wikiPageWikiLink Nickel.
- Buchwald–Hartwig_amination wikiPageWikiLink Nucleophilic_aromatic_substitution.
- Buchwald–Hartwig_amination wikiPageWikiLink Nucleophilic_substitution.
- Buchwald–Hartwig_amination wikiPageWikiLink Organic_chemistry.
- Buchwald–Hartwig_amination wikiPageWikiLink Organotin_chemistry.
- Buchwald–Hartwig_amination wikiPageWikiLink Oxidative_addition.
- Buchwald–Hartwig_amination wikiPageWikiLink Palladium.
- Buchwald–Hartwig_amination wikiPageWikiLink Palladium-catalyzed_coupling_reactions.
- Buchwald–Hartwig_amination wikiPageWikiLink Persistent_carbene.
- Buchwald–Hartwig_amination wikiPageWikiLink Phosphate.
- Buchwald–Hartwig_amination wikiPageWikiLink Phosphine.
- Buchwald–Hartwig_amination wikiPageWikiLink Polar_effect.
- Buchwald–Hartwig_amination wikiPageWikiLink Potassium_tert-butoxide.
- Buchwald–Hartwig_amination wikiPageWikiLink Reaction_mechanism.
- Buchwald–Hartwig_amination wikiPageWikiLink Reductive_amination.
- Buchwald–Hartwig_amination wikiPageWikiLink Reductive_elimination.
- Buchwald–Hartwig_amination wikiPageWikiLink SPANphos.
- Buchwald–Hartwig_amination wikiPageWikiLink Salt_metathesis_reaction.
- Buchwald–Hartwig_amination wikiPageWikiLink Stephen_L._Buchwald.
- Buchwald–Hartwig_amination wikiPageWikiLink Steric_effects.
- Buchwald–Hartwig_amination wikiPageWikiLink Tetrakis(triphenylphosphine)palladium(0).
- Buchwald–Hartwig_amination wikiPageWikiLink Tin.
- Buchwald–Hartwig_amination wikiPageWikiLink Total_synthesis.
- Buchwald–Hartwig_amination wikiPageWikiLink Trifluoromethanesulfonate.
- Buchwald–Hartwig_amination wikiPageWikiLink Ullmann_condensation.
- Buchwald–Hartwig_amination wikiPageWikiLink Xantphos.
- Buchwald–Hartwig_amination wikiPageWikiLink File:BHAFirstgenexamples.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:BHAHetarylamide.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:BHASecondgenchiral.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:BHASecondgenexamples.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:BHAThirdgenscope.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:BHAammonia.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:BHAenolates.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:BHAether.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:Bogerpanekamination.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:Buchwald1994.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:Buchwaldhartwig.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:Hartwig1.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:Migita.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:Monophosmechanism.png.
- Buchwald–Hartwig_amination wikiPageWikiLink File:Tinfree.png.
- Buchwald–Hartwig_amination wikiPageWikiLinkText "Buchwald-Hartwig Cross Coupling".
- Buchwald–Hartwig_amination wikiPageWikiLinkText "Buchwald–Hartwig amination".
- Buchwald–Hartwig_amination wikiPageWikiLinkText "Mechanism".
- Buchwald–Hartwig_amination wikiPageWikiLinkText "Scope".
- Buchwald–Hartwig_amination name "Buchwald-Hartwig amination".
- Buchwald–Hartwig_amination namedafter Stephen_L._Buchwald.
- Buchwald–Hartwig_amination namedafter "John F. Hartwig".
- Buchwald–Hartwig_amination type "Coupling reaction".
- Buchwald–Hartwig_amination wikiPageUsesTemplate Template:Reactionbox.