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- Leimgruber–Batcho_indole_synthesis abstract "The Leimgruber–Batcho indole synthesis is a series of organic reactions that produce indoles from o-nitrotoluenes 1. The first step is the formation of an enamine 2 using N,N-dimethylformamide dimethyl acetal and pyrrolidine. The desired indole 3 is then formed in a second step by reductive cyclisation.In the above scheme, the reductive cyclisation is effected by Raney nickel and hydrazine. Palladium-on-carbon and hydrogen, stannous chloride, sodium hydrosulfite, or iron in acetic acid are also effective reducing agents.".
- Leimgruber–Batcho_indole_synthesis thumbnail Leimgruber-Batcho_Indole_Scheme.png?width=300.
- Leimgruber–Batcho_indole_synthesis wikiPageExternalLink prep.asp?prep=cv7p0034.
- Leimgruber–Batcho_indole_synthesis wikiPageID "2247816".
- Leimgruber–Batcho_indole_synthesis wikiPageLength "4357".
- Leimgruber–Batcho_indole_synthesis wikiPageOutDegree "51".
- Leimgruber–Batcho_indole_synthesis wikiPageRevisionID "679161413".
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Acetic_acid.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Arene_substitution_pattern.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Bartoli_indole_synthesis.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Carbanion.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Category:Carbon-heteroatom_bond_forming_reactions.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Category:Indole_forming_reactions.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Category:Name_reactions.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Chemical_yield.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Conjugated_system.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Deprotonation.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Dimethylamine.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Elimination_reaction.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Enamine.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Fischer_indole_synthesis.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Hydrazine.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Hydrogen.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink In_situ.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Indole.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Iron.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink J._Org._Chem..
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Journal_of_Organic_Chemistry.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Methanol.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Methyl.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Methyl_group.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink N,N-dimethylformamide_dimethyl_acetal.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Nitro_compound.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Nitrogen.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Organic_Syntheses.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Organic_reaction.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Ortho-.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Palladium_on_carbon.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Pharmaceutical.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Pharmaceutical_drug.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Pharmacology.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Polar_effect.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Push–pull_olefin.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Pyrrolidine.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Raney_nickel.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Reagent.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Redox.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Reducing_agent.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Reissert_indole_synthesis.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Sodium_dithionite.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Stannous_chloride.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Tin(II)_chloride.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Toluene.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink Yield_(chemistry).
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink File:Dinitrostyrene_Reductive_Cyclization.png.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLink File:Leimgruber-Batcho_Indole_Scheme.png.
- Leimgruber–Batcho_indole_synthesis wikiPageWikiLinkText "Leimgruber–Batcho indole synthesis".
- Leimgruber–Batcho_indole_synthesis hasPhotoCollection Leimgruber–Batcho_indole_synthesis.
- Leimgruber–Batcho_indole_synthesis wikiPageUsesTemplate Template:DOI.
- Leimgruber–Batcho_indole_synthesis wikiPageUsesTemplate Template:Note.
- Leimgruber–Batcho_indole_synthesis wikiPageUsesTemplate Template:Ref.
- Leimgruber–Batcho_indole_synthesis wikiPageUsesTemplate Template:US_patent.
- Leimgruber–Batcho_indole_synthesis subject Category:Carbon-heteroatom_bond_forming_reactions.
- Leimgruber–Batcho_indole_synthesis subject Category:Indole_forming_reactions.
- Leimgruber–Batcho_indole_synthesis subject Category:Name_reactions.
- Leimgruber–Batcho_indole_synthesis comment "The Leimgruber–Batcho indole synthesis is a series of organic reactions that produce indoles from o-nitrotoluenes 1. The first step is the formation of an enamine 2 using N,N-dimethylformamide dimethyl acetal and pyrrolidine. The desired indole 3 is then formed in a second step by reductive cyclisation.In the above scheme, the reductive cyclisation is effected by Raney nickel and hydrazine.".
- Leimgruber–Batcho_indole_synthesis label "Leimgruber–Batcho indole synthesis".
- Leimgruber–Batcho_indole_synthesis sameAs Synthxc3xa8se_de_Leimgruber-Batcho_de_lindole.
- Leimgruber–Batcho_indole_synthesis sameAs Leimgruber-Batcho-indoolsynthese.
- Leimgruber–Batcho_indole_synthesis sameAs m.06z0s5.
- Leimgruber–Batcho_indole_synthesis sameAs Реакция_Лемгрубера_—_Бачо.
- Leimgruber–Batcho_indole_synthesis sameAs Q2390993.
- Leimgruber–Batcho_indole_synthesis sameAs Q2390993.
- Leimgruber–Batcho_indole_synthesis sameAs Leimgruber-Batcho吲哚合成.
- Leimgruber–Batcho_indole_synthesis wasDerivedFrom Leimgruber–Batcho_indole_synthesis?oldid=679161413.
- Leimgruber–Batcho_indole_synthesis depiction Leimgruber-Batcho_Indole_Scheme.png.
- Leimgruber–Batcho_indole_synthesis isPrimaryTopicOf Leimgruber–Batcho_indole_synthesis.