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- Eschweiler–Clarke_reaction abstract "The Eschweiler–Clarke reaction (also called the Eschweiler–Clarke methylation) is a chemical reaction whereby a primary (or secondary) amine is methylated using excess formic acid and formaldehyde. Reductive amination reactions such as this one will not produce quaternary ammonium salts, but instead will stop at the tertiary amine stage. It is named for the German chemist Wilhelm Eschweiler (1860–1936) and the British chemist Hans Thacher Clarke (1887-1972).".
- Eschweiler–Clarke_reaction thumbnail Eschweiler-Clark_Reaction_Scheme.png?width=300.
- Eschweiler–Clarke_reaction wikiPageID "2032822".
- Eschweiler–Clarke_reaction wikiPageLength "3002".
- Eschweiler–Clarke_reaction wikiPageOutDegree "19".
- Eschweiler–Clarke_reaction wikiPageRevisionID "662809889".
- Eschweiler–Clarke_reaction wikiPageWikiLink Amine.
- Eschweiler–Clarke_reaction wikiPageWikiLink Carbon_dioxide.
- Eschweiler–Clarke_reaction wikiPageWikiLink Category:Methylation.
- Eschweiler–Clarke_reaction wikiPageWikiLink Category:Name_reactions.
- Eschweiler–Clarke_reaction wikiPageWikiLink Category:Organic_redox_reactions.
- Eschweiler–Clarke_reaction wikiPageWikiLink Chemical_reaction.
- Eschweiler–Clarke_reaction wikiPageWikiLink Formaldehyde.
- Eschweiler–Clarke_reaction wikiPageWikiLink Formic_acid.
- Eschweiler–Clarke_reaction wikiPageWikiLink Hans_Thacher_Clarke.
- Eschweiler–Clarke_reaction wikiPageWikiLink Hydride.
- Eschweiler–Clarke_reaction wikiPageWikiLink Imine.
- Eschweiler–Clarke_reaction wikiPageWikiLink Leuckart_reaction.
- Eschweiler–Clarke_reaction wikiPageWikiLink Leuckart–Wallach_reaction.
- Eschweiler–Clarke_reaction wikiPageWikiLink Methylated.
- Eschweiler–Clarke_reaction wikiPageWikiLink Methylation.
- Eschweiler–Clarke_reaction wikiPageWikiLink Redox.
- Eschweiler–Clarke_reaction wikiPageWikiLink Reductive_amination.
- Eschweiler–Clarke_reaction wikiPageWikiLink Sodium_cyanoborohydride.
- Eschweiler–Clarke_reaction wikiPageWikiLink Wilhelm_Eschweiler.
- Eschweiler–Clarke_reaction wikiPageWikiLink File:Eschweiler-Clark_Mechanism.png.
- Eschweiler–Clarke_reaction wikiPageWikiLink File:Eschweiler-Clark_Reaction_Scheme.png.
- Eschweiler–Clarke_reaction wikiPageWikiLinkText "Eschweiler–Clarke reaction".
- Eschweiler–Clarke_reaction wikiPageWikiLinkText "Eschweiler–Clarke".
- Eschweiler–Clarke_reaction hasPhotoCollection Eschweiler–Clarke_reaction.
- Eschweiler–Clarke_reaction wikiPageUsesTemplate Template:Reflist.
- Eschweiler–Clarke_reaction subject Category:Methylation.
- Eschweiler–Clarke_reaction subject Category:Name_reactions.
- Eschweiler–Clarke_reaction subject Category:Organic_redox_reactions.
- Eschweiler–Clarke_reaction comment "The Eschweiler–Clarke reaction (also called the Eschweiler–Clarke methylation) is a chemical reaction whereby a primary (or secondary) amine is methylated using excess formic acid and formaldehyde. Reductive amination reactions such as this one will not produce quaternary ammonium salts, but instead will stop at the tertiary amine stage. It is named for the German chemist Wilhelm Eschweiler (1860–1936) and the British chemist Hans Thacher Clarke (1887-1972).".
- Eschweiler–Clarke_reaction label "Eschweiler–Clarke reaction".
- Eschweiler–Clarke_reaction sameAs Reacció_de_Eschweiler-Clarke.
- Eschweiler–Clarke_reaction sameAs Eschweiler-Clarke-Methylierung.
- Eschweiler–Clarke_reaction sameAs Rxc3xa9action_dEschweiler-Clarke.
- Eschweiler–Clarke_reaction sameAs エシュバイラー・クラーク反応.
- Eschweiler–Clarke_reaction sameAs Eschweiler-Clarke-reactie.
- Eschweiler–Clarke_reaction sameAs m.06gj71.
- Eschweiler–Clarke_reaction sameAs Q731968.
- Eschweiler–Clarke_reaction sameAs Q731968.
- Eschweiler–Clarke_reaction sameAs Eschweiler–Clarke反应.
- Eschweiler–Clarke_reaction wasDerivedFrom Eschweiler–Clarke_reaction?oldid=662809889.
- Eschweiler–Clarke_reaction depiction Eschweiler-Clark_Reaction_Scheme.png.
- Eschweiler–Clarke_reaction isPrimaryTopicOf Eschweiler–Clarke_reaction.