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- Nitrile_anion abstract "Nitrile anions are nitriles lacking a proton at the position α to the nitrile group. They undergo nucleophilic addition and substitution reactions with various electrophiles.Although nitrile anions are functionally similar to enolates, the extra multiple bond in nitrile anions provides them with a unique ketene-like geometry. Additionally, deprotonated cyanohydrins can act as masked acyl anions, giving products impossible to access with enolates alone. The mechanisms of nitrile addition and substitution are well understood; however, strongly basic conditions are usually required, limiting the reaction's synthetic usefulness.".
- Nitrile_anion thumbnail NitrileGen.png?width=300.
- Nitrile_anion wikiPageID "27387883".
- Nitrile_anion wikiPageLength "9927".
- Nitrile_anion wikiPageOutDegree "41".
- Nitrile_anion wikiPageRevisionID "637686533".
- Nitrile_anion wikiPageWikiLink Acyl_chloride.
- Nitrile_anion wikiPageWikiLink Amidine.
- Nitrile_anion wikiPageWikiLink Anyhdride.
- Nitrile_anion wikiPageWikiLink Aryne.
- Nitrile_anion wikiPageWikiLink Benzene.
- Nitrile_anion wikiPageWikiLink Boiling_point.
- Nitrile_anion wikiPageWikiLink Category:Anions.
- Nitrile_anion wikiPageWikiLink Category:Nitriles.
- Nitrile_anion wikiPageWikiLink Category:Reactive_intermediates.
- Nitrile_anion wikiPageWikiLink Cyanohydrin.
- Nitrile_anion wikiPageWikiLink Electrophile.
- Nitrile_anion wikiPageWikiLink Enol.
- Nitrile_anion wikiPageWikiLink Epoxide.
- Nitrile_anion wikiPageWikiLink Ester.
- Nitrile_anion wikiPageWikiLink Ethanol.
- Nitrile_anion wikiPageWikiLink Fractional_distillation.
- Nitrile_anion wikiPageWikiLink Infrared_spectroscopy.
- Nitrile_anion wikiPageWikiLink Ketene.
- Nitrile_anion wikiPageWikiLink Michael_reaction.
- Nitrile_anion wikiPageWikiLink N-Butyllithium.
- Nitrile_anion wikiPageWikiLink Nitrile.
- Nitrile_anion wikiPageWikiLink Nucleophilic_aromatic_substitution.
- Nitrile_anion wikiPageWikiLink Paralobesia_viteana.
- Nitrile_anion wikiPageWikiLink Phase-transfer_catalyst.
- Nitrile_anion wikiPageWikiLink Radical-nucleophilic_aromatic_substitution.
- Nitrile_anion wikiPageWikiLink SN2_reaction.
- Nitrile_anion wikiPageWikiLink Sodium_amide.
- Nitrile_anion wikiPageWikiLink Sodium_carbonate.
- Nitrile_anion wikiPageWikiLink Sodium_hydride.
- Nitrile_anion wikiPageWikiLink Sodium_sulfate.
- Nitrile_anion wikiPageWikiLink Thorpe_reaction.
- Nitrile_anion wikiPageWikiLink Toluene.
- Nitrile_anion wikiPageWikiLink File:NitrileCollin.png.
- Nitrile_anion wikiPageWikiLink File:NitrileEx.png.
- Nitrile_anion wikiPageWikiLink File:NitrileGen.png.
- Nitrile_anion wikiPageWikiLink File:NitrilePTC.png.
- Nitrile_anion wikiPageWikiLink File:NitrileSRN1.png.
- Nitrile_anion wikiPageWikiLink File:NitrileScope.png.
- Nitrile_anion wikiPageWikiLink File:NitrileSynth.png.
- Nitrile_anion wikiPageWikiLink File:Tolunitrile.png.
- Nitrile_anion wikiPageWikiLinkText "Nitrile anion".
- Nitrile_anion wikiPageWikiLinkText "nitrile anion".
- Nitrile_anion wikiPageUsesTemplate Template:Reflist.
- Nitrile_anion subject Category:Anions.
- Nitrile_anion subject Category:Nitriles.
- Nitrile_anion subject Category:Reactive_intermediates.
- Nitrile_anion hypernym Nitriles.
- Nitrile_anion type Group.
- Nitrile_anion type Group.
- Nitrile_anion type Nitrile.
- Nitrile_anion comment "Nitrile anions are nitriles lacking a proton at the position α to the nitrile group. They undergo nucleophilic addition and substitution reactions with various electrophiles.Although nitrile anions are functionally similar to enolates, the extra multiple bond in nitrile anions provides them with a unique ketene-like geometry. Additionally, deprotonated cyanohydrins can act as masked acyl anions, giving products impossible to access with enolates alone.".
- Nitrile_anion label "Nitrile anion".
- Nitrile_anion sameAs Q7041404.
- Nitrile_anion sameAs m.0bxz979.
- Nitrile_anion sameAs Q7041404.
- Nitrile_anion wasDerivedFrom Nitrile_anion?oldid=637686533.
- Nitrile_anion depiction NitrileGen.png.
- Nitrile_anion isPrimaryTopicOf Nitrile_anion.