Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Azide-alkyne_Huisgen_cycloaddition> ?p ?o }
- Azide-alkyne_Huisgen_cycloaddition abstract "The Azide-Alkyne Huisgen Cycloaddition is a 1,3-dipolar cycloaddition between an azide and a terminal or internal alkyne to give a 1,2,3-triazole. Rolf Huisgen was the first to understand the scope of this organic reaction. American chemist K. Barry Sharpless has referred to this cycloaddition as "the cream of the crop" of click chemistry and "the premier example of a click reaction."In the reaction above azide 2 reacts neatly with alkyne 1 to afford the triazole 3 as a mixture of 1,4-adduct and 1,5-adduct at 98 °C in 18 hours.The standard 1,3-cycloaddition between an azide 1,3-dipole and an alkene as dipolarophile has largely been ignored due to lack of reactivity as a result of electron-poor olefins and elimination side reactions. Some success has been found with non-metal-catalyzed cycloadditions, such as the reactions using dipolarophiles that are electron-poor olefins or alkynes. Although azides are not the most reactive 1,3-dipole available for reaction, they are preferred for their relative lack of side reactions and stability in typical synthetic conditions.".
- Azide-alkyne_Huisgen_cycloaddition thumbnail Huisgen.png?width=300.
- Azide-alkyne_Huisgen_cycloaddition wikiPageID "1855478".
- Azide-alkyne_Huisgen_cycloaddition wikiPageLength "17780".
- Azide-alkyne_Huisgen_cycloaddition wikiPageOutDegree "64".
- Azide-alkyne_Huisgen_cycloaddition wikiPageRevisionID "683224556".
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink 1,2,3-Triazole.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink 1,2,3-triazole.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink 1,3-Dipolar_cycloaddition.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink 1,3-dipolar_cycloaddition.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Acetonitrile.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Acetylide.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Activated_complex.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Alkyne.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Amphiphile.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Amphiphilic.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Azide.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Banert_cascade.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Bovine_serum_albumin.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Carbon-nitrogen_bond.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Carbon–nitrogen_bond.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Catalytic_cycle.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Category:Cycloadditions.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Category:Name_reactions.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Chemist.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Click_chemistry.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Conjugated_system.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Cyclic_compound.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Cyclisation.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Cycloaddition.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Cysteine.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink DIPEA.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Degree_of_polymerization.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Density_functional_theory.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Dewar–Chatt–Duncanson_model.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Diameter.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Dimethyl_sulfoxide.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Dimethylformamide.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink End-group.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Fluorene.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Free_radical_polymerization.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink K._Barry_Sharpless.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Karl_Barry_Sharpless.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Ligand.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Micelle.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Morten_Meldal.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Morten_P._Meldal.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink N,N-Diisopropylethylamine.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Nanometer.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Nanometre.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Order_of_reaction.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Organic_reaction.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Oxidative_coupling.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Phenyl.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Phenyl_azide.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Phenyl_group.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Pi_complex.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Polymer.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Polymerization.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Polystyrene.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Protecting_group.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Protonation.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Radical_polymerization.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Rolf_Huisgen.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Ruthenium.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Scripps_Research_Institute.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Second_order_reaction.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Sodium_ascorbate.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Spectator_ligand.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Tetrahydrofuran.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink The_Scripps_Research_Institute.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Thiol.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Toluene.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Transition_metal.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Triethylamine.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Tris(benzyltriazolylmethyl)amine.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink Tris-(benzyltriazolylmethyl)amine.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink File:Clickpolymer.png.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink File:CuAAC_mechanism.png.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink File:Huisgen.png.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLink File:RuAAC_mechanism.png.
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLinkText "Azide-alkyne Huisgen cycloaddition".
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLinkText "CuAAC-click reaction".
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLinkText "Huisgen 1,3-dipolar cycloaddition".
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLinkText "Huisgen cycloaddition".
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLinkText "azide-alkyne Huisgen cycloaddition".
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLinkText "azide-alkyne".
- Azide-alkyne_Huisgen_cycloaddition wikiPageWikiLinkText "huisgen cyclization".
- Azide-alkyne_Huisgen_cycloaddition hasPhotoCollection Azide-alkyne_Huisgen_cycloaddition.
- Azide-alkyne_Huisgen_cycloaddition wikiPageUsesTemplate Template:Reflist.
- Azide-alkyne_Huisgen_cycloaddition subject Category:Cycloadditions.
- Azide-alkyne_Huisgen_cycloaddition subject Category:Name_reactions.
- Azide-alkyne_Huisgen_cycloaddition hypernym Cycloaddition.
- Azide-alkyne_Huisgen_cycloaddition type Eponym.
- Azide-alkyne_Huisgen_cycloaddition type Reaction.
- Azide-alkyne_Huisgen_cycloaddition comment "The Azide-Alkyne Huisgen Cycloaddition is a 1,3-dipolar cycloaddition between an azide and a terminal or internal alkyne to give a 1,2,3-triazole. Rolf Huisgen was the first to understand the scope of this organic reaction. American chemist K.".
- Azide-alkyne_Huisgen_cycloaddition label "Azide-alkyne Huisgen cycloaddition".
- Azide-alkyne_Huisgen_cycloaddition sameAs إضافة_هويزغن_الحلقية_أزيد-ألكاين.
- Azide-alkyne_Huisgen_cycloaddition sameAs Cicloaddizione_di_Huisgen_azide-alchino.
- Azide-alkyne_Huisgen_cycloaddition sameAs Huisgen-1,3-dipolaire_cycloadditie.