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- Hoesch_reaction abstract "The Hoesch reaction or Houben–Hoesch reaction is an organic reaction in which a nitrile reacts with an arene compound to form an aryl ketone. The reaction is a type of Friedel-Crafts acylation with hydrogen chloride and a Lewis acid catalyst.An example is the synthesis of 1-(2,4,6-trihydroxyphenyl)ethanone from phloroglucinol:A ketimine is isolated as an intermediate reaction product. The attacking electrophile is possibly a species of the type R-C+=NHCl−. The arene must be electron-rich i.e. phenol or aniline type. A related reaction is the Gattermann reaction in which hydrocyanic acid not a nitrile is used.The reaction is named after Kurt Hoesch and Josef Houben who reported about this new reaction type in respectively 1915 and 1926.".
- Hoesch_reaction thumbnail Hoesch_reaction_example,_1-(2,4,6-trihydroxyphenyl)ethanone_from_phloroglucinol.png?width=300.
- Hoesch_reaction wikiPageID "16437233".
- Hoesch_reaction wikiPageLength "2405".
- Hoesch_reaction wikiPageOutDegree "18".
- Hoesch_reaction wikiPageRevisionID "705819391".
- Hoesch_reaction wikiPageWikiLink Aromatic_hydrocarbon.
- Hoesch_reaction wikiPageWikiLink Catalysis.
- Hoesch_reaction wikiPageWikiLink Category:Name_reactions.
- Hoesch_reaction wikiPageWikiLink Category:Substitution_reactions.
- Hoesch_reaction wikiPageWikiLink Electrophile.
- Hoesch_reaction wikiPageWikiLink Friedel–Crafts_reaction.
- Hoesch_reaction wikiPageWikiLink Gattermann_reaction.
- Hoesch_reaction wikiPageWikiLink Hydrogen_chloride.
- Hoesch_reaction wikiPageWikiLink Imine.
- Hoesch_reaction wikiPageWikiLink Josef_Houben.
- Hoesch_reaction wikiPageWikiLink Ketone.
- Hoesch_reaction wikiPageWikiLink Lewis_acids_and_bases.
- Hoesch_reaction wikiPageWikiLink Nitrile.
- Hoesch_reaction wikiPageWikiLink Organic_reaction.
- Hoesch_reaction wikiPageWikiLink Phloroglucinol.
- Hoesch_reaction wikiPageWikiLink File:Hoesch_reaction_example,_1-(2,4,6-trihydroxyphenyl)ethanone_from_phloroglucinol.png.
- Hoesch_reaction wikiPageWikiLink File:Hoesch_reaction_mechanism.png.
- Hoesch_reaction wikiPageWikiLinkText "Hoesch reaction".
- Hoesch_reaction name "Houben–Hoesch reaction".
- Hoesch_reaction namedafter Josef_Houben.
- Hoesch_reaction namedafter "Kurt Hoesch".
- Hoesch_reaction type "Coupling reaction".
- Hoesch_reaction wikiPageUsesTemplate Template:Reactionbox.
- Hoesch_reaction wikiPageUsesTemplate Template:Reflist.
- Hoesch_reaction subject Category:Name_reactions.
- Hoesch_reaction subject Category:Substitution_reactions.
- Hoesch_reaction hypernym Reaction.
- Hoesch_reaction type Disease.
- Hoesch_reaction type Eponym.
- Hoesch_reaction type Reaction.
- Hoesch_reaction comment "The Hoesch reaction or Houben–Hoesch reaction is an organic reaction in which a nitrile reacts with an arene compound to form an aryl ketone. The reaction is a type of Friedel-Crafts acylation with hydrogen chloride and a Lewis acid catalyst.An example is the synthesis of 1-(2,4,6-trihydroxyphenyl)ethanone from phloroglucinol:A ketimine is isolated as an intermediate reaction product. The attacking electrophile is possibly a species of the type R-C+=NHCl−. The arene must be electron-rich i.e.".
- Hoesch_reaction label "Hoesch reaction".
- Hoesch_reaction sameAs Q5876506.
- Hoesch_reaction sameAs Houben-Hoesch-Reaktion.
- Hoesch_reaction sameAs Reacción_de_Hoesch.
- Hoesch_reaction sameAs واکنش_هوبن–هش.
- Hoesch_reaction sameAs m.03y1vdp.
- Hoesch_reaction sameAs Реакция_Губена_—_Гёша.
- Hoesch_reaction sameAs Houben–Hoescheva_reakcija.
- Hoesch_reaction sameAs ஓய்சிஃசு_வினை.
- Hoesch_reaction sameAs Q5876506.
- Hoesch_reaction sameAs Hoesch反应.
- Hoesch_reaction wasDerivedFrom Hoesch_reaction?oldid=705819391.
- Hoesch_reaction depiction Hoesch_reaction_example,_1-(2,4,6-trihydroxyphenyl)ethanone_from_phloroglucinol.png.
- Hoesch_reaction isPrimaryTopicOf Hoesch_reaction.