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- Nitrone-olefin_3+2_cycloaddition abstract "The nitrone-olefin (3+2) cycloaddition reaction is the combination of a nitrone with an alkene or alkyne to generate an isoxazoline or isoxazolidine via a (3+2) cycloaddition process. This reaction is a 1,3-dipolar cycloaddition, in which the nitrone acts as the 1,3-dipole, and the alkene or alkyne as the dipolarophile.".
- Nitrone-olefin_3+2_cycloaddition thumbnail NitrGen.png?width=300.
- Nitrone-olefin_3+2_cycloaddition wikiPageID "27613618".
- Nitrone-olefin_3+2_cycloaddition wikiPageLength "7374".
- Nitrone-olefin_3+2_cycloaddition wikiPageOutDegree "27".
- Nitrone-olefin_3+2_cycloaddition wikiPageRevisionID "693335448".
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink 1,3-Dipolar_cycloaddition.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink 1,3-dipole.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Acetylide.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Alkene.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Alkyne.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Baylis–Hillman_reaction.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Category:Cycloadditions.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Category:Heterocycle_forming_reactions.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Copper.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Cycloaddition.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Isoxazoline.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Lupinine.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Nitrone.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Oxazolidine.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink Β-Lactam.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink File:Kinugasa_reaction.png.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink File:NitrGen.png.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink File:NitrMech4.png.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink File:NitrScope1.png.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink File:NitrScope2.png.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink File:NitrScope3.png.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink File:NitrScope4.png.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink File:NitrScope5.png.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink File:NitrSynth1.png.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink File:NitrSynth2.png.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLink File:NitrSynth3.png.
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLinkText "Nitrone-olefin 3+2 cycloaddition".
- Nitrone-olefin_3+2_cycloaddition wikiPageWikiLinkText "Nitrone-olefin cycloaddition".
- Nitrone-olefin_3+2_cycloaddition wikiPageUsesTemplate Template:Correct_title.
- Nitrone-olefin_3+2_cycloaddition wikiPageUsesTemplate Template:Reflist.
- Nitrone-olefin_3+2_cycloaddition subject Category:Cycloadditions.
- Nitrone-olefin_3+2_cycloaddition subject Category:Heterocycle_forming_reactions.
- Nitrone-olefin_3+2_cycloaddition hypernym Combination.
- Nitrone-olefin_3+2_cycloaddition type Drug.
- Nitrone-olefin_3+2_cycloaddition type Reaction.
- Nitrone-olefin_3+2_cycloaddition comment "The nitrone-olefin (3+2) cycloaddition reaction is the combination of a nitrone with an alkene or alkyne to generate an isoxazoline or isoxazolidine via a (3+2) cycloaddition process. This reaction is a 1,3-dipolar cycloaddition, in which the nitrone acts as the 1,3-dipole, and the alkene or alkyne as the dipolarophile.".
- Nitrone-olefin_3+2_cycloaddition label "Nitrone-olefin 3+2 cycloaddition".
- Nitrone-olefin_3+2_cycloaddition sameAs Q7041489.
- Nitrone-olefin_3+2_cycloaddition sameAs m.09db3s.
- Nitrone-olefin_3+2_cycloaddition sameAs m.0dll8kk.
- Nitrone-olefin_3+2_cycloaddition sameAs Q7041489.
- Nitrone-olefin_3+2_cycloaddition wasDerivedFrom Nitrone-olefin_3+2_cycloaddition?oldid=693335448.
- Nitrone-olefin_3+2_cycloaddition depiction NitrGen.png.
- Nitrone-olefin_3+2_cycloaddition isPrimaryTopicOf Nitrone-olefin_3+2_cycloaddition.