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- 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 wikiPageRevisionID "601827068".
- Azide-alkyne_Huisgen_cycloaddition hasPhotoCollection Azide-alkyne_Huisgen_cycloaddition.
- Azide-alkyne_Huisgen_cycloaddition subject Category:Cycloadditions.
- Azide-alkyne_Huisgen_cycloaddition subject Category:Name_reactions.
- Azide-alkyne_Huisgen_cycloaddition type ChemicalProcess113446390.
- Azide-alkyne_Huisgen_cycloaddition type ChemicalReaction113447361.
- Azide-alkyne_Huisgen_cycloaddition type NameReactions.
- Azide-alkyne_Huisgen_cycloaddition type NaturalProcess113518963.
- Azide-alkyne_Huisgen_cycloaddition type PhysicalEntity100001930.
- Azide-alkyne_Huisgen_cycloaddition type Process100029677.
- 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 label "Cicloaddizione di Huisgen azide-alchino".
- Azide-alkyne_Huisgen_cycloaddition label "Huisgen-1,3-dipolaire cycloadditie".
- Azide-alkyne_Huisgen_cycloaddition label "Азид-алкиновое циклоприсоединение".
- Azide-alkyne_Huisgen_cycloaddition label "إضافة هويزن 3,1-ثنائية القطبية الحلقية".
- Azide-alkyne_Huisgen_cycloaddition sameAs Cicloaddizione_di_Huisgen_azide-alchino.
- Azide-alkyne_Huisgen_cycloaddition sameAs Huisgen-1,3-dipolaire_cycloadditie.
- Azide-alkyne_Huisgen_cycloaddition sameAs m.061bpd.
- Azide-alkyne_Huisgen_cycloaddition sameAs Q4950309.
- Azide-alkyne_Huisgen_cycloaddition sameAs Q4950309.
- Azide-alkyne_Huisgen_cycloaddition sameAs Azide-alkyne_Huisgen_cycloaddition.
- Azide-alkyne_Huisgen_cycloaddition wasDerivedFrom Azide-alkyne_Huisgen_cycloaddition?oldid=601827068.
- Azide-alkyne_Huisgen_cycloaddition depiction Huisgen.png.
- Azide-alkyne_Huisgen_cycloaddition isPrimaryTopicOf Azide-alkyne_Huisgen_cycloaddition.