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- Bischler–Napieralski_reaction abstract "The Bischler–Napieralski reaction is an intramolecular electrophilic aromatic substitution reaction that allows for the cyclization of β-arylethylamides or β-arylethylcarbamates. It was first discovered in 1893 by August Bischler and Bernard Napieralski, in affiliation with Basle Chemical Works and the University of Zurich. The reaction is most notably used in the synthesis of dihydroisoquinolines, which can be subsequently oxidized to isoquinolines.".
- Bischler–Napieralski_reaction thumbnail Bischler-Napieralski_Reaction_Scheme.png?width=300.
- Bischler–Napieralski_reaction wikiPageExternalLink f756.table.
- Bischler–Napieralski_reaction wikiPageID "2589104".
- Bischler–Napieralski_reaction wikiPageLength "8690".
- Bischler–Napieralski_reaction wikiPageOutDegree "49".
- Bischler–Napieralski_reaction wikiPageRevisionID "681379644".
- Bischler–Napieralski_reaction wikiPageWikiLink Acetal.
- Bischler–Napieralski_reaction wikiPageWikiLink Aldehyde.
- Bischler–Napieralski_reaction wikiPageWikiLink Amide.
- Bischler–Napieralski_reaction wikiPageWikiLink Aryl.
- Bischler–Napieralski_reaction wikiPageWikiLink August_Bischler.
- Bischler–Napieralski_reaction wikiPageWikiLink Basel.
- Bischler–Napieralski_reaction wikiPageWikiLink Benzene.
- Bischler–Napieralski_reaction wikiPageWikiLink Bischler–Napieralski_reaction.
- Bischler–Napieralski_reaction wikiPageWikiLink Boron_trifluoride.
- Bischler–Napieralski_reaction wikiPageWikiLink Carbonyl.
- Bischler–Napieralski_reaction wikiPageWikiLink Category:Heterocycle_forming_reactions.
- Bischler–Napieralski_reaction wikiPageWikiLink Category:Name_reactions.
- Bischler–Napieralski_reaction wikiPageWikiLink Chemische_Berichte.
- Bischler–Napieralski_reaction wikiPageWikiLink Condensation.
- Bischler–Napieralski_reaction wikiPageWikiLink Cyclic_compound.
- Bischler–Napieralski_reaction wikiPageWikiLink Desiccant.
- Bischler–Napieralski_reaction wikiPageWikiLink Electron-donating.
- Bischler–Napieralski_reaction wikiPageWikiLink Electrophilic_aromatic_substitution.
- Bischler–Napieralski_reaction wikiPageWikiLink Elimination_reaction.
- Bischler–Napieralski_reaction wikiPageWikiLink Imidoyl_chloride.
- Bischler–Napieralski_reaction wikiPageWikiLink Imine.
- Bischler–Napieralski_reaction wikiPageWikiLink Isoquinoline.
- Bischler–Napieralski_reaction wikiPageWikiLink Lewis_acids_and_bases.
- Bischler–Napieralski_reaction wikiPageWikiLink Nitro_compound.
- Bischler–Napieralski_reaction wikiPageWikiLink Organic_redox_reaction.
- Bischler–Napieralski_reaction wikiPageWikiLink Phenanthridine.
- Bischler–Napieralski_reaction wikiPageWikiLink Phosphoric_acids_and_phosphates.
- Bischler–Napieralski_reaction wikiPageWikiLink Phosphorus_pentoxide.
- Bischler–Napieralski_reaction wikiPageWikiLink Phosphoryl_chloride.
- Bischler–Napieralski_reaction wikiPageWikiLink Pictet–Spengler_reaction.
- Bischler–Napieralski_reaction wikiPageWikiLink Pomeranz–Fritsch_reaction.
- Bischler–Napieralski_reaction wikiPageWikiLink Reflux.
- Bischler–Napieralski_reaction wikiPageWikiLink Springer_Science+Business_Media.
- Bischler–Napieralski_reaction wikiPageWikiLink Substitution_reaction.
- Bischler–Napieralski_reaction wikiPageWikiLink Tin(IV)_chloride.
- Bischler–Napieralski_reaction wikiPageWikiLink Trifluoromethanesulfonic_anhydride.
- Bischler–Napieralski_reaction wikiPageWikiLink University_of_Zurich.
- Bischler–Napieralski_reaction wikiPageWikiLink File:BNR_rxn_imine-ester_mechanism.svg.
- Bischler–Napieralski_reaction wikiPageWikiLink File:BNR_rxn_nitrilium_mechanism.svg.
- Bischler–Napieralski_reaction wikiPageWikiLink File:BNR_variation.svg.
- Bischler–Napieralski_reaction wikiPageWikiLink File:Bischler-Napieralski_Reaction_Scheme.png.
- Bischler–Napieralski_reaction wikiPageWikiLink File:Pictet-Gams_reaction.svg.
- Bischler–Napieralski_reaction wikiPageWikiLinkText "Bischler–Napieralski reaction".
- Bischler–Napieralski_reaction wikiPageWikiLinkText "Bischler–Napieralski reaction#Pictet–Gams reaction".
- Bischler–Napieralski_reaction name "Bischler-Napieralski reaction".
- Bischler–Napieralski_reaction namedafter August_Bischler.
- Bischler–Napieralski_reaction namedafter "Bernard Napieralski".
- Bischler–Napieralski_reaction type "Ring forming reaction".
- Bischler–Napieralski_reaction wikiPageUsesTemplate Template:Cite_book.
- Bischler–Napieralski_reaction wikiPageUsesTemplate Template:Cite_journal.
- Bischler–Napieralski_reaction wikiPageUsesTemplate Template:Reactionbox.
- Bischler–Napieralski_reaction wikiPageUsesTemplate Template:Reactionbox_Identifiers.
- Bischler–Napieralski_reaction wikiPageUsesTemplate Template:Reflist.
- Bischler–Napieralski_reaction subject Category:Heterocycle_forming_reactions.
- Bischler–Napieralski_reaction subject Category:Name_reactions.
- Bischler–Napieralski_reaction hypernym Reaction.
- Bischler–Napieralski_reaction type Disease.
- Bischler–Napieralski_reaction type Eponym.
- Bischler–Napieralski_reaction type Reaction.
- Bischler–Napieralski_reaction type Redirect.
- Bischler–Napieralski_reaction comment "The Bischler–Napieralski reaction is an intramolecular electrophilic aromatic substitution reaction that allows for the cyclization of β-arylethylamides or β-arylethylcarbamates. It was first discovered in 1893 by August Bischler and Bernard Napieralski, in affiliation with Basle Chemical Works and the University of Zurich. The reaction is most notably used in the synthesis of dihydroisoquinolines, which can be subsequently oxidized to isoquinolines.".
- Bischler–Napieralski_reaction label "Bischler–Napieralski reaction".
- Bischler–Napieralski_reaction sameAs Q866098.
- Bischler–Napieralski_reaction sameAs Bischler-Napieralski-Reaktion.
- Bischler–Napieralski_reaction sameAs ビシュラー・ナピエラルスキー反応.
- Bischler–Napieralski_reaction sameAs Bischler-Napieralski-reactie.
- Bischler–Napieralski_reaction sameAs Reação_de_Bischler-Napieralski.
- Bischler–Napieralski_reaction sameAs m.07q21h.
- Bischler–Napieralski_reaction sameAs Q866098.
- Bischler–Napieralski_reaction sameAs 比施勒-纳皮耶拉尔斯基反应.
- Bischler–Napieralski_reaction wasDerivedFrom Bischler–Napieralski_reaction?oldid=681379644.
- Bischler–Napieralski_reaction depiction Bischler-Napieralski_Reaction_Scheme.png.
- Bischler–Napieralski_reaction isPrimaryTopicOf Bischler–Napieralski_reaction.