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- Horner–Wadsworth–Emmons_reaction abstract "The Horner–Wadsworth–Emmons reaction (or HWE reaction) is a chemical reaction used in organic chemistry of stabilized phosphonate carbanions with aldehydes (or ketones) to produce predominantly E-alkenes.In 1958, Leopold Horner published a modified Wittig reaction using phosphonate-stabilized carbanions. William S. Wadsworth and William D. Emmons further defined the reaction.In contrast to phosphonium ylides used in the Wittig reaction, phosphonate-stabilized carbanions are more nucleophilic but less basic. Likewise, phosphonate-stabilized carbanions can be alkylated. Unlike phosphonium ylides, the dialkylphosphate salt byproduct is easily removed by aqueous extraction.Several reviews have been published.".
- Horner–Wadsworth–Emmons_reaction thumbnail Horner-Wadsworth-Emmons_Reaction_Example.png?width=300.
- Horner–Wadsworth–Emmons_reaction wikiPageID "3804552".
- Horner–Wadsworth–Emmons_reaction wikiPageLength "8475".
- Horner–Wadsworth–Emmons_reaction wikiPageOutDegree "60".
- Horner–Wadsworth–Emmons_reaction wikiPageRevisionID "683048463".
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink 1,8-Diazabicycloundec-7-ene.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink 18-Crown-6.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink 18-crown-6.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Aldehyde.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Alkene.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Aqueous.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Aqueous_solution.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Aromatic.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Aromaticity.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Carbanion.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Category:Carbon-carbon_bond_forming_reactions.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Category:Name_reactions.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Chemical_equilibrium.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Chemical_reaction.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Clayton_Heathcock.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink DBU_(chemistry).
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Deprotonation.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Diisopropylcarbodiimide.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Dimethoxyethane.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Electron-withdrawing_group.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Elimination_reaction.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Ethyl_group.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Halide.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Isomer.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Isopropyl.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Ketone.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Leopold_Horner.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Liquid-liquid_extraction.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Liquid–liquid_extraction.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Lithium.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Lithium_chloride.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Magnesium.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Methyl.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Methyl_group.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Michaelis–Arbuzov_reaction.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Michaelis–Becker_reaction.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink N,N-Diisopropylcarbodiimide.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Nucleophile.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Nucleophilic.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Nucleophilic_addition.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Organic_chemistry.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Peterson_olefination.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Peterson_reaction.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Phosphonate.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Phosphonium_ylide.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Polar_effect.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Potassium.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Potassium_bis(trimethylsilyl)amide.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Potassium_hexamethyldisilazide.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Rate-determining_step.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Rate-limiting_step.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Sodium.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Sodium_hydride.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Stereochemical.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Stereochemistry.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Tebbe_olefination.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Tebbes_reagent.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Tetrahydrofuran.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Triethylamine.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink W._Clark_Still.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink William_D._Emmons.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink William_S._Wadsworth.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink Wittig_reaction.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink File:Horner-Wadsworth-Emmons_Branched_Example.svg.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink File:Horner-Wadsworth-Emmons_Reaction_Example.png.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink File:Horner-Wadsworth-Emmons_Still_Example.png.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLink File:„Horner-Wadsworth-Emmons-Mechanism“V1.svg.
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLinkText "Horner-Wadsworth-Emmons Olefination".
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLinkText "Horner–Wadsworth–Emmons (HWE) reaction".
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLinkText "Horner–Wadsworth–Emmons reaction".
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLinkText "Horner–Wadsworth–Emmons reaction#Still modification".
- Horner–Wadsworth–Emmons_reaction wikiPageWikiLinkText "olefination reagent".
- Horner–Wadsworth–Emmons_reaction hasPhotoCollection Horner–Wadsworth–Emmons_reaction.
- Horner–Wadsworth–Emmons_reaction wikiPageUsesTemplate Template:Reflist.
- Horner–Wadsworth–Emmons_reaction wikiPageUsesTemplate Template:Use_dmy_dates.
- Horner–Wadsworth–Emmons_reaction subject Category:Carbon-carbon_bond_forming_reactions.
- Horner–Wadsworth–Emmons_reaction subject Category:Name_reactions.
- Horner–Wadsworth–Emmons_reaction comment "The Horner–Wadsworth–Emmons reaction (or HWE reaction) is a chemical reaction used in organic chemistry of stabilized phosphonate carbanions with aldehydes (or ketones) to produce predominantly E-alkenes.In 1958, Leopold Horner published a modified Wittig reaction using phosphonate-stabilized carbanions. William S. Wadsworth and William D.".
- Horner–Wadsworth–Emmons_reaction label "Horner–Wadsworth–Emmons reaction".
- Horner–Wadsworth–Emmons_reaction sameAs Horner-Wadsworth-Emmons-Reaktion.
- Horner–Wadsworth–Emmons_reaction sameAs Reazione_di_Horner-Wadsworth-Emmons.
- Horner–Wadsworth–Emmons_reaction sameAs ホーナー・ワズワース・エモンズ反応.
- Horner–Wadsworth–Emmons_reaction sameAs Horner-Wadsworth-Emmons-reactie.
- Horner–Wadsworth–Emmons_reaction sameAs m.0b0wb5.
- Horner–Wadsworth–Emmons_reaction sameAs Реакція_Хорнера_—_Водсворта_—_Еммонса.
- Horner–Wadsworth–Emmons_reaction sameAs Q905020.
- Horner–Wadsworth–Emmons_reaction sameAs Q905020.
- Horner–Wadsworth–Emmons_reaction sameAs Horner–Wadsworth–Emmons反应.
- Horner–Wadsworth–Emmons_reaction wasDerivedFrom Horner–Wadsworth–Emmons_reaction?oldid=683048463.
- Horner–Wadsworth–Emmons_reaction depiction Horner-Wadsworth-Emmons_Reaction_Example.png.
- Horner–Wadsworth–Emmons_reaction isPrimaryTopicOf Horner–Wadsworth–Emmons_reaction.