Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Azomethine_ylide> ?p ?o }
- Azomethine_ylide abstract "Azomethine ylides are nitrogen-based 1,3-dipoles, consisting of an iminium ion next to a carbanion. They are used in 1,3-dipolar cycloaddition reactions to form 5-membered heterocycles, including pyrrolidines and pyrrolines. These reactions are highly stereo- and regioselective, and have the potential to form four new contiguous stereocenters. Azomethine ylides thus have high utility in total synthesis, and formation of chiral ligands and pharmaceuticals. Azomethine ylides can be generated from many sources, including aziridines, imines, and iminiums. They are often generated in situ, and immediately reacted with dipolarophiles.".
- Azomethine_ylide thumbnail Azomethine_ylide.png?width=300.
- Azomethine_ylide wikiPageID "3359945".
- Azomethine_ylide wikiPageLength "18213".
- Azomethine_ylide wikiPageOutDegree "74".
- Azomethine_ylide wikiPageRevisionID "674985659".
- Azomethine_ylide wikiPageWikiLink 1,3-Dipolar_cycloaddition.
- Azomethine_ylide wikiPageWikiLink 1,3-dipolar_cycloaddition.
- Azomethine_ylide wikiPageWikiLink 1,3-dipole.
- Azomethine_ylide wikiPageWikiLink Aldehyde.
- Azomethine_ylide wikiPageWikiLink Alkene.
- Azomethine_ylide wikiPageWikiLink Alkylation.
- Azomethine_ylide wikiPageWikiLink Alkyne.
- Azomethine_ylide wikiPageWikiLink Amine.
- Azomethine_ylide wikiPageWikiLink Antarafacial_and_suprafacial.
- Azomethine_ylide wikiPageWikiLink Aziridine.
- Azomethine_ylide wikiPageWikiLink Aziridines.
- Azomethine_ylide wikiPageWikiLink Carbanion.
- Azomethine_ylide wikiPageWikiLink Carbonyl.
- Azomethine_ylide wikiPageWikiLink Carboxylic_acid.
- Azomethine_ylide wikiPageWikiLink Category:Organic_chemistry.
- Azomethine_ylide wikiPageWikiLink Chiral_ligand.
- Azomethine_ylide wikiPageWikiLink Concerted_reaction.
- Azomethine_ylide wikiPageWikiLink Conjugated_system.
- Azomethine_ylide wikiPageWikiLink Conrotatory.
- Azomethine_ylide wikiPageWikiLink Conrotatory_and_disrotatory.
- Azomethine_ylide wikiPageWikiLink Decarboxylation.
- Azomethine_ylide wikiPageWikiLink Deprotonation.
- Azomethine_ylide wikiPageWikiLink Diels–Alder_reaction.
- Azomethine_ylide wikiPageWikiLink Electrocyclic_reaction.
- Azomethine_ylide wikiPageWikiLink Electrocyclization.
- Azomethine_ylide wikiPageWikiLink Enantioselective_synthesis.
- Azomethine_ylide wikiPageWikiLink Fullerene.
- Azomethine_ylide wikiPageWikiLink HOMO.
- Azomethine_ylide wikiPageWikiLink LUMO.
- Azomethine_ylide wikiPageWikiLink Heterocycle.
- Azomethine_ylide wikiPageWikiLink Heterocyclic_compound.
- Azomethine_ylide wikiPageWikiLink Iminium.
- Azomethine_ylide wikiPageWikiLink Intramolecular.
- Azomethine_ylide wikiPageWikiLink Intramolecular_reaction.
- Azomethine_ylide wikiPageWikiLink Mesoionic.
- Azomethine_ylide wikiPageWikiLink Metal_phosphine_complex.
- Azomethine_ylide wikiPageWikiLink Münchnone.
- Azomethine_ylide wikiPageWikiLink Oxazolidine.
- Azomethine_ylide wikiPageWikiLink Pharmaceutical_drug.
- Azomethine_ylide wikiPageWikiLink Pharmaceuticals.
- Azomethine_ylide wikiPageWikiLink Pi_stacking.
- Azomethine_ylide wikiPageWikiLink Polar_effect.
- Azomethine_ylide wikiPageWikiLink Prochiral.
- Azomethine_ylide wikiPageWikiLink Prochirality.
- Azomethine_ylide wikiPageWikiLink Prototropy.
- Azomethine_ylide wikiPageWikiLink Pyrrolidine.
- Azomethine_ylide wikiPageWikiLink Pyrrolidines.
- Azomethine_ylide wikiPageWikiLink Pyrroline.
- Azomethine_ylide wikiPageWikiLink Pyrrolines.
- Azomethine_ylide wikiPageWikiLink Regioselective.
- Azomethine_ylide wikiPageWikiLink Regioselectivity.
- Azomethine_ylide wikiPageWikiLink Resonance_(chemistry).
- Azomethine_ylide wikiPageWikiLink Resonance_structure.
- Azomethine_ylide wikiPageWikiLink Spiro_compound.
- Azomethine_ylide wikiPageWikiLink Spirocycle.
- Azomethine_ylide wikiPageWikiLink Stacking_(chemistry).
- Azomethine_ylide wikiPageWikiLink Stereoselectivity.
- Azomethine_ylide wikiPageWikiLink Suprafacial.
- Azomethine_ylide wikiPageWikiLink Tautomer.
- Azomethine_ylide wikiPageWikiLink Torquoselectivity.
- Azomethine_ylide wikiPageWikiLink Total_synthesis.
- Azomethine_ylide wikiPageWikiLink Woodward-Hoffman_rules.
- Azomethine_ylide wikiPageWikiLink Woodward–Hoffmann_rules.
- Azomethine_ylide wikiPageWikiLink Ylide.
- Azomethine_ylide wikiPageWikiLink Ylides.
- Azomethine_ylide wikiPageWikiLink File:Application_of_azomethine_ylide_in_the_synthesis_of_spirotryprostatin.tif.
- Azomethine_ylide wikiPageWikiLink File:Aziridine_opening.png.
- Azomethine_ylide wikiPageWikiLink File:Azomethine_ylide.png.
- Azomethine_ylide wikiPageWikiLink File:Azomethine_ylide_cycloaddition.png.
- Azomethine_ylide wikiPageWikiLink File:Azomethine_ylide_cycloaddition_rxn.png.
- Azomethine_ylide wikiPageWikiLink File:Azomethine_ylide_from_condensation.png.
- Azomethine_ylide wikiPageWikiLink File:Azomethine_ylide_from_imine.png.
- Azomethine_ylide wikiPageWikiLink File:Azomethine_ylide_from_munchnone.png.
- Azomethine_ylide wikiPageWikiLink File:Azomethine_ylide_resonance.png.
- Azomethine_ylide wikiPageWikiLink File:Azomethine_ylide_shapes.png.
- Azomethine_ylide wikiPageWikiLink File:Benzodiazepinones_from_azomethine_ylides.png.
- Azomethine_ylide wikiPageWikiLink File:Deprotonation_of_iminium.png.
- Azomethine_ylide wikiPageWikiLink File:Synthesis_of_Martinellic_acid.svg.
- Azomethine_ylide wikiPageWikiLink File:Ylide_1,7_electrocyclization.png.
- Azomethine_ylide wikiPageWikiLinkText "Azomethine ylide".
- Azomethine_ylide wikiPageWikiLinkText "azomethine ylide".
- Azomethine_ylide hasPhotoCollection Azomethine_ylide.
- Azomethine_ylide wikiPageUsesTemplate Template:Main.
- Azomethine_ylide wikiPageUsesTemplate Template:Reflist.
- Azomethine_ylide wikiPageUsesTemplate Template:See_also.
- Azomethine_ylide subject Category:Organic_chemistry.
- Azomethine_ylide hypernym Dipoles.
- Azomethine_ylide type Thing.
- Azomethine_ylide comment "Azomethine ylides are nitrogen-based 1,3-dipoles, consisting of an iminium ion next to a carbanion. They are used in 1,3-dipolar cycloaddition reactions to form 5-membered heterocycles, including pyrrolidines and pyrrolines. These reactions are highly stereo- and regioselective, and have the potential to form four new contiguous stereocenters. Azomethine ylides thus have high utility in total synthesis, and formation of chiral ligands and pharmaceuticals.".
- Azomethine_ylide label "Azomethine ylide".
- Azomethine_ylide seeAlso Aziridine.
- Azomethine_ylide seeAlso 3-dipole_formation.
- Azomethine_ylide sameAs Iluros_de_azometina.
- Azomethine_ylide sameAs m.0zg7433.