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- Gomberg–Bachmann_reaction abstract "The Gomberg–Bachmann reaction, named for the Ukrainian-American chemist Moses Gomberg and the American chemist Werner Emmanuel Bachmann, is an aryl-aryl coupling reaction via a diazonium salt.Gomberg-Bachmann reactionThe arene compound 1 (here benzene) is coupled with base with the diazonium salt 2 to the biaryl 3 through an intermediate aryl radical. For example, p-bromobiphenyl may be prepared from 4-bromoaniline and benzene: BrC6H4NH2 + C6H6 → BrC6H4−C6H5The reaction offers a wide scope for both diazonium component and arene component but yields are generally low following the original procedure (less than 40%), given the many side-reactions of diazonium salts. Several improvements have been suggested. One possibility is to employ diazonium tetrafluoroborates in arene solvent together with a phase-transfer catalyst, another is to use 1-aryl-3,3-dialkyltriazenes.".
- Gomberg–Bachmann_reaction thumbnail Gombergalg.png?width=300.
- Gomberg–Bachmann_reaction wikiPageID "7022785".
- Gomberg–Bachmann_reaction wikiPageLength "4000".
- Gomberg–Bachmann_reaction wikiPageOutDegree "20".
- Gomberg–Bachmann_reaction wikiPageRevisionID "674368484".
- Gomberg–Bachmann_reaction wikiPageWikiLink 4-Bromoaniline.
- Gomberg–Bachmann_reaction wikiPageWikiLink Aromatic_hydrocarbon.
- Gomberg–Bachmann_reaction wikiPageWikiLink Aryl.
- Gomberg–Bachmann_reaction wikiPageWikiLink Aryl_radical.
- Gomberg–Bachmann_reaction wikiPageWikiLink Benzene.
- Gomberg–Bachmann_reaction wikiPageWikiLink Carbazole.
- Gomberg–Bachmann_reaction wikiPageWikiLink Category:Name_reactions.
- Gomberg–Bachmann_reaction wikiPageWikiLink Category:Substitution_reactions.
- Gomberg–Bachmann_reaction wikiPageWikiLink Coupling_reaction.
- Gomberg–Bachmann_reaction wikiPageWikiLink Diazonium_compound.
- Gomberg–Bachmann_reaction wikiPageWikiLink Fluorenone.
- Gomberg–Bachmann_reaction wikiPageWikiLink Intramolecular_reaction.
- Gomberg–Bachmann_reaction wikiPageWikiLink Meerwein_arylation.
- Gomberg–Bachmann_reaction wikiPageWikiLink Moses_Gomberg.
- Gomberg–Bachmann_reaction wikiPageWikiLink Sandmeyer_reaction.
- Gomberg–Bachmann_reaction wikiPageWikiLink Werner_Emmanuel_Bachmann.
- Gomberg–Bachmann_reaction wikiPageWikiLink File:Gombergalg.png.
- Gomberg–Bachmann_reaction wikiPageWikiLink File:PschorrReaction.svg.
- Gomberg–Bachmann_reaction wikiPageWikiLinkText "Gomberg–Bachmann reaction".
- Gomberg–Bachmann_reaction subject Category:Name_reactions.
- Gomberg–Bachmann_reaction subject Category:Substitution_reactions.
- Gomberg–Bachmann_reaction hypernym Reaction.
- Gomberg–Bachmann_reaction type Disease.
- Gomberg–Bachmann_reaction type Eponym.
- Gomberg–Bachmann_reaction type Reaction.
- Gomberg–Bachmann_reaction type Redirect.
- Gomberg–Bachmann_reaction comment "The Gomberg–Bachmann reaction, named for the Ukrainian-American chemist Moses Gomberg and the American chemist Werner Emmanuel Bachmann, is an aryl-aryl coupling reaction via a diazonium salt.Gomberg-Bachmann reactionThe arene compound 1 (here benzene) is coupled with base with the diazonium salt 2 to the biaryl 3 through an intermediate aryl radical.".
- Gomberg–Bachmann_reaction label "Gomberg–Bachmann reaction".
- Gomberg–Bachmann_reaction sameAs Q903787.
- Gomberg–Bachmann_reaction sameAs Gomberg-Bachmann-Reaktion.
- Gomberg–Bachmann_reaction sameAs Reacción_de_Gomberg-Bachmann.
- Gomberg–Bachmann_reaction sameAs واکنش_گومبرگ–باخمان.
- Gomberg–Bachmann_reaction sameAs Reazione_di_Gomberg-Bachmann.
- Gomberg–Bachmann_reaction sameAs ゴンバーグ・バックマン反応.
- Gomberg–Bachmann_reaction sameAs Gomberg-Bachmann-reactie.
- Gomberg–Bachmann_reaction sameAs m.0h0sf8.
- Gomberg–Bachmann_reaction sameAs Q903787.
- Gomberg–Bachmann_reaction sameAs 冈伯格-巴赫曼反应.
- Gomberg–Bachmann_reaction wasDerivedFrom Gomberg–Bachmann_reaction?oldid=674368484.
- Gomberg–Bachmann_reaction depiction Gombergalg.png.
- Gomberg–Bachmann_reaction isPrimaryTopicOf Gomberg–Bachmann_reaction.