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- Doebner–Miller_reaction abstract "The Doebner–Miller reaction is the organic reaction of an aniline with α,β-unsaturated carbonyl compounds to form quinolines.This reaction is also known as the Skraup-Doebner-Von Miller quinoline synthesis, and is named after the Czech chemist Zdenko Hans Skraup (1850–1910), and the Germans Oscar Döbner (Doebner) (1850–1907) and Wilhelm von Miller (1848–1899). When the α,β-unsaturated carbonyl compound is prepared in situ from two carbonyl compounds (via an Aldol condensation), the reaction is known as the Beyer method for quinolines.The reaction is catalyzed by Lewis acids such as tin tetrachloride and scandium(III) triflate and Brønsted acids such as p-toluenesulfonic acid, perchloric acid, amberlite and iodine.".
- Doebner–Miller_reaction thumbnail Doebner-Miller_Reaction_Scheme.png?width=300.
- Doebner–Miller_reaction wikiPageID "4123943".
- Doebner–Miller_reaction wikiPageLength "4704".
- Doebner–Miller_reaction wikiPageOutDegree "44".
- Doebner–Miller_reaction wikiPageRevisionID "593389862".
- Doebner–Miller_reaction wikiPageWikiLink Aldol_condensation.
- Doebner–Miller_reaction wikiPageWikiLink Amberlite.
- Doebner–Miller_reaction wikiPageWikiLink Amine.
- Doebner–Miller_reaction wikiPageWikiLink Aniline.
- Doebner–Miller_reaction wikiPageWikiLink Brønsted_acid.
- Doebner–Miller_reaction wikiPageWikiLink Brønsted–Lowry_acid–base_theory.
- Doebner–Miller_reaction wikiPageWikiLink Carbon-14.
- Doebner–Miller_reaction wikiPageWikiLink Carbonyl.
- Doebner–Miller_reaction wikiPageWikiLink Category:Condensation_reactions.
- Doebner–Miller_reaction wikiPageWikiLink Category:Name_reactions.
- Doebner–Miller_reaction wikiPageWikiLink Category:Quinoline_forming_reactions.
- Doebner–Miller_reaction wikiPageWikiLink Combes_quinoline_synthesis.
- Doebner–Miller_reaction wikiPageWikiLink Condensation_reaction.
- Doebner–Miller_reaction wikiPageWikiLink Conjugated_system.
- Doebner–Miller_reaction wikiPageWikiLink Cyclohexanone.
- Doebner–Miller_reaction wikiPageWikiLink Doebner_reaction.
- Doebner–Miller_reaction wikiPageWikiLink Electrophilic_addition.
- Doebner–Miller_reaction wikiPageWikiLink Elimination_reaction.
- Doebner–Miller_reaction wikiPageWikiLink Enol.
- Doebner–Miller_reaction wikiPageWikiLink Gould–Jacobs_reaction.
- Doebner–Miller_reaction wikiPageWikiLink Imine.
- Doebner–Miller_reaction wikiPageWikiLink In_situ.
- Doebner–Miller_reaction wikiPageWikiLink Iodine.
- Doebner–Miller_reaction wikiPageWikiLink Knorr_quinoline_synthesis.
- Doebner–Miller_reaction wikiPageWikiLink Lewis_acid.
- Doebner–Miller_reaction wikiPageWikiLink Lewis_acids_and_bases.
- Doebner–Miller_reaction wikiPageWikiLink Mass_spectrometry.
- Doebner–Miller_reaction wikiPageWikiLink Nucleophilic_conjugate_addition.
- Doebner–Miller_reaction wikiPageWikiLink Organic_reaction.
- Doebner–Miller_reaction wikiPageWikiLink Oscar_Döbner.
- Doebner–Miller_reaction wikiPageWikiLink P-Toluenesulfonic_acid.
- Doebner–Miller_reaction wikiPageWikiLink Perchloric_acid.
- Doebner–Miller_reaction wikiPageWikiLink Pulegone.
- Doebner–Miller_reaction wikiPageWikiLink Quinoline.
- Doebner–Miller_reaction wikiPageWikiLink Reaction_mechanism.
- Doebner–Miller_reaction wikiPageWikiLink Reversible_reaction.
- Doebner–Miller_reaction wikiPageWikiLink Scandium(III)_triflate.
- Doebner–Miller_reaction wikiPageWikiLink Scandium(III)_trifluoromethanesulfonate.
- Doebner–Miller_reaction wikiPageWikiLink Skraup_reaction.
- Doebner–Miller_reaction wikiPageWikiLink Skraup_synthesis.
- Doebner–Miller_reaction wikiPageWikiLink Tin(IV)_chloride.
- Doebner–Miller_reaction wikiPageWikiLink Tin_tetrachloride.
- Doebner–Miller_reaction wikiPageWikiLink Wilhelm_von_Miller.
- Doebner–Miller_reaction wikiPageWikiLink Zdenko_Hans_Skraup.
- Doebner–Miller_reaction wikiPageWikiLink Α,β-unsaturated_carbonyl_compound.
- Doebner–Miller_reaction wikiPageWikiLink File:Doebner-Miller_Reaction_Scheme.png.
- Doebner–Miller_reaction wikiPageWikiLink File:Skraup_mechanism.png.
- Doebner–Miller_reaction wikiPageWikiLinkText "Doebner–Miller reaction".
- Doebner–Miller_reaction hasPhotoCollection Doebner–Miller_reaction.
- Doebner–Miller_reaction wikiPageUsesTemplate Template:Reflist.
- Doebner–Miller_reaction subject Category:Condensation_reactions.
- Doebner–Miller_reaction subject Category:Name_reactions.
- Doebner–Miller_reaction subject Category:Quinoline_forming_reactions.
- Doebner–Miller_reaction comment "The Doebner–Miller reaction is the organic reaction of an aniline with α,β-unsaturated carbonyl compounds to form quinolines.This reaction is also known as the Skraup-Doebner-Von Miller quinoline synthesis, and is named after the Czech chemist Zdenko Hans Skraup (1850–1910), and the Germans Oscar Döbner (Doebner) (1850–1907) and Wilhelm von Miller (1848–1899).".
- Doebner–Miller_reaction label "Doebner–Miller reaction".
- Doebner–Miller_reaction sameAs Doebner-Miller-Reaktion.
- Doebner–Miller_reaction sameAs Reacción_de_Doebner-Miller.
- Doebner–Miller_reaction sameAs Doebner-Miller-reactie.
- Doebner–Miller_reaction sameAs m.0bkbty.
- Doebner–Miller_reaction sameAs Q1058053.
- Doebner–Miller_reaction sameAs Q1058053.
- Doebner–Miller_reaction sameAs 德布纳-米勒反应.
- Doebner–Miller_reaction wasDerivedFrom Doebner–Miller_reaction?oldid=593389862.
- Doebner–Miller_reaction depiction Doebner-Miller_Reaction_Scheme.png.
- Doebner–Miller_reaction isPrimaryTopicOf Doebner–Miller_reaction.