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- Reimer–Tiemann_reaction abstract "The Reimer–Tiemann reaction is a chemical reaction used for the ortho-formylation of phenols; with the simplest example being the conversion of phenol to salicylaldehyde. The reaction was discovered by Karl Reimer and Ferdinand Tiemann. The Reimer in question was Karl Reimer (1845-1883) not the less known Carl Ludwig Reimer (1856-1921).".
- Reimer–Tiemann_reaction thumbnail Reimer-Tiemann_Reaction_Scheme.png?width=300.
- Reimer–Tiemann_reaction wikiPageID "3094935".
- Reimer–Tiemann_reaction wikiPageLength "5978".
- Reimer–Tiemann_reaction wikiPageOutDegree "44".
- Reimer–Tiemann_reaction wikiPageRevisionID "705090199".
- Reimer–Tiemann_reaction wikiPageWikiLink 1,4-Dioxane.
- Reimer–Tiemann_reaction wikiPageWikiLink Acid.
- Reimer–Tiemann_reaction wikiPageWikiLink Anhydrous.
- Reimer–Tiemann_reaction wikiPageWikiLink Arene_substitution_pattern.
- Reimer–Tiemann_reaction wikiPageWikiLink Aromaticity.
- Reimer–Tiemann_reaction wikiPageWikiLink Carbon_tetrachloride.
- Reimer–Tiemann_reaction wikiPageWikiLink Carbylamine_reaction.
- Reimer–Tiemann_reaction wikiPageWikiLink Category:Addition_reactions.
- Reimer–Tiemann_reaction wikiPageWikiLink Category:Carbon-carbon_bond_forming_reactions.
- Reimer–Tiemann_reaction wikiPageWikiLink Category:Formylation_reactions.
- Reimer–Tiemann_reaction wikiPageWikiLink Category:Name_reactions.
- Reimer–Tiemann_reaction wikiPageWikiLink Chemical_compound.
- Reimer–Tiemann_reaction wikiPageWikiLink Chemical_reaction.
- Reimer–Tiemann_reaction wikiPageWikiLink Chemical_synthesis.
- Reimer–Tiemann_reaction wikiPageWikiLink Chloroform.
- Reimer–Tiemann_reaction wikiPageWikiLink Dichlorocarbene.
- Reimer–Tiemann_reaction wikiPageWikiLink Duff_reaction.
- Reimer–Tiemann_reaction wikiPageWikiLink Electrophilic_aromatic_substitution.
- Reimer–Tiemann_reaction wikiPageWikiLink Emulsion.
- Reimer–Tiemann_reaction wikiPageWikiLink Ferdinand_Tiemann.
- Reimer–Tiemann_reaction wikiPageWikiLink Formylation.
- Reimer–Tiemann_reaction wikiPageWikiLink Formylation_reaction.
- Reimer–Tiemann_reaction wikiPageWikiLink Gattermann_reaction.
- Reimer–Tiemann_reaction wikiPageWikiLink Hydroxide.
- Reimer–Tiemann_reaction wikiPageWikiLink Karl_Reimer.
- Reimer–Tiemann_reaction wikiPageWikiLink Multiphasic_liquid.
- Reimer–Tiemann_reaction wikiPageWikiLink Phase-transfer_catalyst.
- Reimer–Tiemann_reaction wikiPageWikiLink Phenol.
- Reimer–Tiemann_reaction wikiPageWikiLink Phenolic_acid.
- Reimer–Tiemann_reaction wikiPageWikiLink Salicylaldehyde.
- Reimer–Tiemann_reaction wikiPageWikiLink Salicylic_acid.
- Reimer–Tiemann_reaction wikiPageWikiLink Substrate_(chemistry).
- Reimer–Tiemann_reaction wikiPageWikiLink Thermal_runaway.
- Reimer–Tiemann_reaction wikiPageWikiLink Vilsmeier–Haack_reaction.
- Reimer–Tiemann_reaction wikiPageWikiLink File:Reimer-Tiemann_Reaction_Mechanism.png.
- Reimer–Tiemann_reaction wikiPageWikiLink File:Reimer-Tiemann_Reaction_Scheme.png.
- Reimer–Tiemann_reaction wikiPageWikiLinkText "Reimer–Tiemann reaction".
- Reimer–Tiemann_reaction name "Reimer-Tiemann reaction".
- Reimer–Tiemann_reaction namedafter "Ferdinand Tiemann".
- Reimer–Tiemann_reaction namedafter "Karl Reimer".
- Reimer–Tiemann_reaction type "Addition reaction".
- Reimer–Tiemann_reaction wikiPageUsesTemplate Template:Reactionbox.
- Reimer–Tiemann_reaction wikiPageUsesTemplate Template:Reactionbox_Identifiers.
- Reimer–Tiemann_reaction wikiPageUsesTemplate Template:Reflist.
- Reimer–Tiemann_reaction subject Category:Addition_reactions.
- Reimer–Tiemann_reaction subject Category:Carbon-carbon_bond_forming_reactions.
- Reimer–Tiemann_reaction subject Category:Formylation_reactions.
- Reimer–Tiemann_reaction subject Category:Name_reactions.
- Reimer–Tiemann_reaction hypernym Reaction.
- Reimer–Tiemann_reaction type Disease.
- Reimer–Tiemann_reaction type Eponym.
- Reimer–Tiemann_reaction type Reaction.
- Reimer–Tiemann_reaction type Redirect.
- Reimer–Tiemann_reaction comment "The Reimer–Tiemann reaction is a chemical reaction used for the ortho-formylation of phenols; with the simplest example being the conversion of phenol to salicylaldehyde. The reaction was discovered by Karl Reimer and Ferdinand Tiemann. The Reimer in question was Karl Reimer (1845-1883) not the less known Carl Ludwig Reimer (1856-1921).".
- Reimer–Tiemann_reaction label "Reimer–Tiemann reaction".
- Reimer–Tiemann_reaction sameAs Q899663.
- Reimer–Tiemann_reaction sameAs Reacció_de_Reimer–Tiemann.
- Reimer–Tiemann_reaction sameAs Reimer-Tiemann-Reaktion.
- Reimer–Tiemann_reaction sameAs واکنش_رایمر-تیمان.
- Reimer–Tiemann_reaction sameAs Reimer–Tiemann-reaktio.
- Reimer–Tiemann_reaction sameAs Réaction_de_Reimer-Tiemann.
- Reimer–Tiemann_reaction sameAs ライマー・チーマン反応.
- Reimer–Tiemann_reaction sameAs Reimer-Tiemann-reactie.
- Reimer–Tiemann_reaction sameAs Reakcja_Reimera-Tiemanna.
- Reimer–Tiemann_reaction sameAs Reação_de_Reimer-Tiemann.
- Reimer–Tiemann_reaction sameAs m.08r224.
- Reimer–Tiemann_reaction sameAs Реакция_Раймера_—_Тимана.
- Reimer–Tiemann_reaction sameAs Ример-Тајманова_реакција.
- Reimer–Tiemann_reaction sameAs Q899663.
- Reimer–Tiemann_reaction sameAs 瑞穆尔-悌曼反应.
- Reimer–Tiemann_reaction wasDerivedFrom Reimer–Tiemann_reaction?oldid=705090199.
- Reimer–Tiemann_reaction depiction Reimer-Tiemann_Reaction_Scheme.png.
- Reimer–Tiemann_reaction isPrimaryTopicOf Reimer–Tiemann_reaction.