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- Bamford–Stevens_reaction abstract "The Bamford–Stevens reaction is a chemical reaction whereby treatment of tosylhydrazones with strong base gives alkenes. It is named for the British chemist William Randall Bamford and the Scottish chemist Thomas Stevens Stevens (1900–2000). The usage of aprotic solvents gives predominantly Z-alkenes, while protic solvent gives a mixture of E- and Z-alkenes. As an alkene-generating transformation, the Bamford–Stevens reaction has broad utility in synthetic methodology and complex molecule synthesis.The treatment of tosylhydrazones with alkyl lithium reagents is called the Shapiro reaction.".
- Bamford–Stevens_reaction thumbnail Bamford-Stevens_Reaction_Scheme.png?width=300.
- Bamford–Stevens_reaction wikiPageID "1918370".
- Bamford–Stevens_reaction wikiPageLength "13625".
- Bamford–Stevens_reaction wikiPageOutDegree "47".
- Bamford–Stevens_reaction wikiPageRevisionID "678362087".
- Bamford–Stevens_reaction wikiPageWikiLink Alkene.
- Bamford–Stevens_reaction wikiPageWikiLink Annulation.
- Bamford–Stevens_reaction wikiPageWikiLink Aprotic_solvent.
- Bamford–Stevens_reaction wikiPageWikiLink Aromatic.
- Bamford–Stevens_reaction wikiPageWikiLink Aromaticity.
- Bamford–Stevens_reaction wikiPageWikiLink Aryne.
- Bamford–Stevens_reaction wikiPageWikiLink Beta-Hydride_elimination.
- Bamford–Stevens_reaction wikiPageWikiLink Beta-hydride_elimination.
- Bamford–Stevens_reaction wikiPageWikiLink Beta-silicon_effect.
- Bamford–Stevens_reaction wikiPageWikiLink Carbenium_ion.
- Bamford–Stevens_reaction wikiPageWikiLink Category:Elimination_reactions.
- Bamford–Stevens_reaction wikiPageWikiLink Category:Name_reactions.
- Bamford–Stevens_reaction wikiPageWikiLink Chemical_reaction.
- Bamford–Stevens_reaction wikiPageWikiLink Claisen_rearrangement.
- Bamford–Stevens_reaction wikiPageWikiLink Coupling_reaction.
- Bamford–Stevens_reaction wikiPageWikiLink Coupling_reactions.
- Bamford–Stevens_reaction wikiPageWikiLink Cycloaddition.
- Bamford–Stevens_reaction wikiPageWikiLink Decarboxylation.
- Bamford–Stevens_reaction wikiPageWikiLink Diene.
- Bamford–Stevens_reaction wikiPageWikiLink Electrophile.
- Bamford–Stevens_reaction wikiPageWikiLink Electrophilic.
- Bamford–Stevens_reaction wikiPageWikiLink Heterocyclic_compound.
- Bamford–Stevens_reaction wikiPageWikiLink Hydride_shift.
- Bamford–Stevens_reaction wikiPageWikiLink Krapcho_decarboxylation.
- Bamford–Stevens_reaction wikiPageWikiLink Migratory_insertion.
- Bamford–Stevens_reaction wikiPageWikiLink Nucleophile.
- Bamford–Stevens_reaction wikiPageWikiLink Nucleophilic.
- Bamford–Stevens_reaction wikiPageWikiLink Organometallic.
- Bamford–Stevens_reaction wikiPageWikiLink Organometallic_chemistry.
- Bamford–Stevens_reaction wikiPageWikiLink Oxidative_addition.
- Bamford–Stevens_reaction wikiPageWikiLink Protic_solvent.
- Bamford–Stevens_reaction wikiPageWikiLink Shapiro_reaction.
- Bamford–Stevens_reaction wikiPageWikiLink Sigmatropic_reaction.
- Bamford–Stevens_reaction wikiPageWikiLink Silicon.
- Bamford–Stevens_reaction wikiPageWikiLink Stereoelectronic_effect.
- Bamford–Stevens_reaction wikiPageWikiLink Thomas_Stevens_Stevens.
- Bamford–Stevens_reaction wikiPageWikiLink Tosylhydrazone.
- Bamford–Stevens_reaction wikiPageWikiLink Total_synthesis.
- Bamford–Stevens_reaction wikiPageWikiLink William_Randall_Bamford.
- Bamford–Stevens_reaction wikiPageWikiLink File:Application_of_the_Bamford-Stevens_reaction_in_natural_product_total_synthesis.jpg.
- Bamford–Stevens_reaction wikiPageWikiLink File:Bamford-Stevens_MechanismA.png.
- Bamford–Stevens_reaction wikiPageWikiLink File:Bamford-Stevens_MechanismB.png.
- Bamford–Stevens_reaction wikiPageWikiLink File:Bamford-Stevens_MechanismC.png.
- Bamford–Stevens_reaction wikiPageWikiLink File:Bamford-Stevens_Reaction_Scheme.png.
- Bamford–Stevens_reaction wikiPageWikiLink File:Mechanism_of_the_Pd-catalyzed_reaction_of_N-tosylhydrazones_with_aryl_halides.jpg.
- Bamford–Stevens_reaction wikiPageWikiLink File:Metal-free_cross-coupling_reaction_with_N-tosylhydrazones_and_boronic_acids.jpg.
- Bamford–Stevens_reaction wikiPageWikiLink File:N-tosylhydrazones_as_Reagents_for_Cross-Coupling_Reactions.jpg.
- Bamford–Stevens_reaction wikiPageWikiLink File:Rhodium-catalyzed_tandem_Bamford-Stevens_Thermal_Aliphatic_Claisen_Reaction.jpg.
- Bamford–Stevens_reaction wikiPageWikiLink File:Silicon-directed_Bamford-Stevens_reaction_of_β-Trimethylsilyl_N-aziridinylimines.jpg.
- Bamford–Stevens_reaction wikiPageWikiLink File:Synthesis_of_3-Substituted_Indazoles_from_Arynes_and_N-tosylhydrazones.png.
- Bamford–Stevens_reaction wikiPageWikiLinkText "Bamford–Stevens reaction".
- Bamford–Stevens_reaction hasPhotoCollection Bamford–Stevens_reaction.
- Bamford–Stevens_reaction subject Category:Elimination_reactions.
- Bamford–Stevens_reaction subject Category:Name_reactions.
- Bamford–Stevens_reaction comment "The Bamford–Stevens reaction is a chemical reaction whereby treatment of tosylhydrazones with strong base gives alkenes. It is named for the British chemist William Randall Bamford and the Scottish chemist Thomas Stevens Stevens (1900–2000). The usage of aprotic solvents gives predominantly Z-alkenes, while protic solvent gives a mixture of E- and Z-alkenes.".
- Bamford–Stevens_reaction label "Bamford–Stevens reaction".
- Bamford–Stevens_reaction sameAs Bamford-Stevens-Reaktion.
- Bamford–Stevens_reaction sameAs Reacción_de_Bamford-Stevens.
- Bamford–Stevens_reaction sameAs バンフォード・スティーブンス反応.
- Bamford–Stevens_reaction sameAs m.0660fc.
- Bamford–Stevens_reaction sameAs Q575939.
- Bamford–Stevens_reaction sameAs Q575939.
- Bamford–Stevens_reaction sameAs 班福德-史蒂文斯反应.
- Bamford–Stevens_reaction wasDerivedFrom Bamford–Stevens_reaction?oldid=678362087.
- Bamford–Stevens_reaction depiction Bamford-Stevens_Reaction_Scheme.png.
- Bamford–Stevens_reaction isPrimaryTopicOf Bamford–Stevens_reaction.