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- Friedländer_synthesis abstract "The Friedländer synthesis is a chemical reaction of 2-aminobenzaldehydes with ketones to form quinoline derivatives. It is named after German chemist Paul Friedländer (1857–1923).This reaction has been catalyzed by trifluoroacetic acid, toluenesulfonic acid, iodine, and Lewis acids.Several reviews have been published.".
- Friedländer_synthesis thumbnail Friedlaender_Synthesis_Scheme_V.1.svg?width=300.
- Friedländer_synthesis wikiPageID "3240259".
- Friedländer_synthesis wikiPageLength "4120".
- Friedländer_synthesis wikiPageOutDegree "25".
- Friedländer_synthesis wikiPageRevisionID "593391547".
- Friedländer_synthesis wikiPageWikiLink Aldol_reaction.
- Friedländer_synthesis wikiPageWikiLink Carbonyl.
- Friedländer_synthesis wikiPageWikiLink Category:Condensation_reactions.
- Friedländer_synthesis wikiPageWikiLink Category:Name_reactions.
- Friedländer_synthesis wikiPageWikiLink Category:Quinoline_forming_reactions.
- Friedländer_synthesis wikiPageWikiLink Chemical_reaction.
- Friedländer_synthesis wikiPageWikiLink Doebner-Miller_reaction.
- Friedländer_synthesis wikiPageWikiLink Doebner–Miller_reaction.
- Friedländer_synthesis wikiPageWikiLink Elimination_reaction.
- Friedländer_synthesis wikiPageWikiLink Imine.
- Friedländer_synthesis wikiPageWikiLink Iodine.
- Friedländer_synthesis wikiPageWikiLink Ketone.
- Friedländer_synthesis wikiPageWikiLink Lewis_acid.
- Friedländer_synthesis wikiPageWikiLink Lewis_acids_and_bases.
- Friedländer_synthesis wikiPageWikiLink Niementowski_quinoline_synthesis.
- Friedländer_synthesis wikiPageWikiLink P-Toluenesulfonic_acid.
- Friedländer_synthesis wikiPageWikiLink Paul_Friedländer_(chemist).
- Friedländer_synthesis wikiPageWikiLink Pfitzinger_reaction.
- Friedländer_synthesis wikiPageWikiLink Povarov_reaction.
- Friedländer_synthesis wikiPageWikiLink Quinoline.
- Friedländer_synthesis wikiPageWikiLink Rate-determining_step.
- Friedländer_synthesis wikiPageWikiLink Rate-limiting_step.
- Friedländer_synthesis wikiPageWikiLink Reaction_mechanism.
- Friedländer_synthesis wikiPageWikiLink Schiff_base.
- Friedländer_synthesis wikiPageWikiLink Skraup_reaction.
- Friedländer_synthesis wikiPageWikiLink Toluenesulfonic_acid.
- Friedländer_synthesis wikiPageWikiLink Trifluoroacetic_acid.
- Friedländer_synthesis wikiPageWikiLink Α,β-unsaturated_carbonyl_compound.
- Friedländer_synthesis wikiPageWikiLink File:Friedlaender_Synthesis_Scheme_V.1.svg.
- Friedländer_synthesis wikiPageWikiLink File:FriedlanderReactionMechanism.svg.
- Friedländer_synthesis wikiPageWikiLinkText "Friedlander quinolone synthesis".
- Friedländer_synthesis wikiPageWikiLinkText "Friedländer synthesis".
- Friedländer_synthesis hasPhotoCollection Friedländer_synthesis.
- Friedländer_synthesis wikiPageUsesTemplate Template:Reflist.
- Friedländer_synthesis wikiPageUsesTemplate Template:Use_dmy_dates.
- Friedländer_synthesis subject Category:Condensation_reactions.
- Friedländer_synthesis subject Category:Name_reactions.
- Friedländer_synthesis subject Category:Quinoline_forming_reactions.
- Friedländer_synthesis comment "The Friedländer synthesis is a chemical reaction of 2-aminobenzaldehydes with ketones to form quinoline derivatives. It is named after German chemist Paul Friedländer (1857–1923).This reaction has been catalyzed by trifluoroacetic acid, toluenesulfonic acid, iodine, and Lewis acids.Several reviews have been published.".
- Friedländer_synthesis label "Friedländer synthesis".
- Friedländer_synthesis sameAs Friedländer-Chinolin-Synthese.
- Friedländer_synthesis sameAs Síntesis_de_quinolinas_de_Friedländer.
- Friedländer_synthesis sameAs Friedländer-synthese.
- Friedländer_synthesis sameAs m.090lx1.
- Friedländer_synthesis sameAs Q1058388.
- Friedländer_synthesis sameAs Q1058388.
- Friedländer_synthesis sameAs 弗里德兰德喹啉合成反应.
- Friedländer_synthesis wasDerivedFrom Friedländer_synthesis?oldid=593391547.
- Friedländer_synthesis depiction Friedlaender_Synthesis_Scheme_V.1.svg.
- Friedländer_synthesis isPrimaryTopicOf Friedländer_synthesis.