Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Nucleophilic_conjugate_addition> ?p ?o }
- Nucleophilic_conjugate_addition abstract "Nucleophilic conjugate addition is a type of organic reaction. Ordinary nucleophilic additions or 1,2-nucleophilic additions deal mostly with additions to carbonyl compounds. Simple alkene compounds do not show 1,2 reactivity due to lack of polarity, unless the alkene is activated with special substituents. With α,β-unsaturated carbonyl compounds such as cyclohexenone it can be deduced from resonance structures that the β position is an electrophilic site which can react with a nucleophile. The negative charge in these structures is stored as an alkoxide anion. Such a nucleophilic addition is called a nucleophilic conjugate addition or 1,4-nucleophilic addition. The most important active alkenes are the aforementioned conjugated carbonyls and acrylonitriles.".
- Nucleophilic_conjugate_addition thumbnail NucleophilicConjugateAddition.svg?width=300.
- Nucleophilic_conjugate_addition wikiPageExternalLink 16248643.
- Nucleophilic_conjugate_addition wikiPageID "3082178".
- Nucleophilic_conjugate_addition wikiPageLength "5985".
- Nucleophilic_conjugate_addition wikiPageOutDegree "72".
- Nucleophilic_conjugate_addition wikiPageRevisionID "635337424".
- Nucleophilic_conjugate_addition wikiPageWikiLink Acetylacetonate.
- Nucleophilic_conjugate_addition wikiPageWikiLink Acetylacetone.
- Nucleophilic_conjugate_addition wikiPageWikiLink Acrylonitrile.
- Nucleophilic_conjugate_addition wikiPageWikiLink Alkene.
- Nucleophilic_conjugate_addition wikiPageWikiLink Alkoxide.
- Nucleophilic_conjugate_addition wikiPageWikiLink Alkylimino-de-oxo-bisubstitution.
- Nucleophilic_conjugate_addition wikiPageWikiLink Amine.
- Nucleophilic_conjugate_addition wikiPageWikiLink Asymmetric_synthesis.
- Nucleophilic_conjugate_addition wikiPageWikiLink BINAP.
- Nucleophilic_conjugate_addition wikiPageWikiLink Carbanion.
- Nucleophilic_conjugate_addition wikiPageWikiLink Carbon-carbon_bond.
- Nucleophilic_conjugate_addition wikiPageWikiLink Carbonyl.
- Nucleophilic_conjugate_addition wikiPageWikiLink Carbon–carbon_bond.
- Nucleophilic_conjugate_addition wikiPageWikiLink Cascade_reaction.
- Nucleophilic_conjugate_addition wikiPageWikiLink Catalysis.
- Nucleophilic_conjugate_addition wikiPageWikiLink Catalyst.
- Nucleophilic_conjugate_addition wikiPageWikiLink Category:Addition_reactions.
- Nucleophilic_conjugate_addition wikiPageWikiLink Chemical_polarity.
- Nucleophilic_conjugate_addition wikiPageWikiLink Chiral_auxiliary.
- Nucleophilic_conjugate_addition wikiPageWikiLink Chiral_ligand.
- Nucleophilic_conjugate_addition wikiPageWikiLink Chirality_(chemistry).
- Nucleophilic_conjugate_addition wikiPageWikiLink Conjugated_system.
- Nucleophilic_conjugate_addition wikiPageWikiLink Cyclohexenone.
- Nucleophilic_conjugate_addition wikiPageWikiLink Diethyl_azodicarboxylate.
- Nucleophilic_conjugate_addition wikiPageWikiLink Diethylaluminium_cyanide.
- Nucleophilic_conjugate_addition wikiPageWikiLink Diethylaluminum_cyanide.
- Nucleophilic_conjugate_addition wikiPageWikiLink Dimethyl_fumarate.
- Nucleophilic_conjugate_addition wikiPageWikiLink Domino_reaction.
- Nucleophilic_conjugate_addition wikiPageWikiLink Electrophile.
- Nucleophilic_conjugate_addition wikiPageWikiLink Enamine.
- Nucleophilic_conjugate_addition wikiPageWikiLink Enantiomer.
- Nucleophilic_conjugate_addition wikiPageWikiLink Enantiomeric_excess.
- Nucleophilic_conjugate_addition wikiPageWikiLink Enantioselective.
- Nucleophilic_conjugate_addition wikiPageWikiLink Enantioselective_synthesis.
- Nucleophilic_conjugate_addition wikiPageWikiLink Enol.
- Nucleophilic_conjugate_addition wikiPageWikiLink Enolate.
- Nucleophilic_conjugate_addition wikiPageWikiLink Enone.
- Nucleophilic_conjugate_addition wikiPageWikiLink Furan.
- Nucleophilic_conjugate_addition wikiPageWikiLink Gilman_reagent.
- Nucleophilic_conjugate_addition wikiPageWikiLink Glutathione.
- Nucleophilic_conjugate_addition wikiPageWikiLink Hydrocyanation_of_unsaturated_carbonyl_compounds.
- Nucleophilic_conjugate_addition wikiPageWikiLink Hydrocyanation_of_unsaturated_carbonyls.
- Nucleophilic_conjugate_addition wikiPageWikiLink Hydrogen_cyanide.
- Nucleophilic_conjugate_addition wikiPageWikiLink Imidazolidinone.
- Nucleophilic_conjugate_addition wikiPageWikiLink Iminium.
- Nucleophilic_conjugate_addition wikiPageWikiLink J._Am._Chem._Soc..
- Nucleophilic_conjugate_addition wikiPageWikiLink J._Braz._Chem._Soc..
- Nucleophilic_conjugate_addition wikiPageWikiLink Journal_of_the_American_Chemical_Society.
- Nucleophilic_conjugate_addition wikiPageWikiLink Keto-enol_tautomerism.
- Nucleophilic_conjugate_addition wikiPageWikiLink Keto–enol_tautomerism.
- Nucleophilic_conjugate_addition wikiPageWikiLink Methyl_vinyl_ketone.
- Nucleophilic_conjugate_addition wikiPageWikiLink Methylamine.
- Nucleophilic_conjugate_addition wikiPageWikiLink Methylvinylketone.
- Nucleophilic_conjugate_addition wikiPageWikiLink Michael_reaction.
- Nucleophilic_conjugate_addition wikiPageWikiLink Multi-component_reaction.
- Nucleophilic_conjugate_addition wikiPageWikiLink Nucleophile.
- Nucleophilic_conjugate_addition wikiPageWikiLink Nucleophilic.
- Nucleophilic_conjugate_addition wikiPageWikiLink Nucleophilic_abstraction.
- Nucleophilic_conjugate_addition wikiPageWikiLink Nucleophilic_addition.
- Nucleophilic_conjugate_addition wikiPageWikiLink Organic_reaction.
- Nucleophilic_conjugate_addition wikiPageWikiLink Organometallic.
- Nucleophilic_conjugate_addition wikiPageWikiLink Organometallic_chemistry.
- Nucleophilic_conjugate_addition wikiPageWikiLink Organozinc.
- Nucleophilic_conjugate_addition wikiPageWikiLink Organozinc_compound.
- Nucleophilic_conjugate_addition wikiPageWikiLink Phenylboronic_acid.
- Nucleophilic_conjugate_addition wikiPageWikiLink Protonation.
- Nucleophilic_conjugate_addition wikiPageWikiLink Quinone.
- Nucleophilic_conjugate_addition wikiPageWikiLink Resonance_(chemistry).
- Nucleophilic_conjugate_addition wikiPageWikiLink Resonance_structure.
- Nucleophilic_conjugate_addition wikiPageWikiLink Rhodium.
- Nucleophilic_conjugate_addition wikiPageWikiLink Secondary_amine.
- Nucleophilic_conjugate_addition wikiPageWikiLink Stork_enamine_alkylation.
- Nucleophilic_conjugate_addition wikiPageWikiLink Stork_enamine_reaction.
- Nucleophilic_conjugate_addition wikiPageWikiLink Substituent.
- Nucleophilic_conjugate_addition wikiPageWikiLink Syn_addition.
- Nucleophilic_conjugate_addition wikiPageWikiLink Syn_and_anti_addition.
- Nucleophilic_conjugate_addition wikiPageWikiLink Thiol.
- Nucleophilic_conjugate_addition wikiPageWikiLink Vicinal_difunctionalization.
- Nucleophilic_conjugate_addition wikiPageWikiLink Vinylogous.
- Nucleophilic_conjugate_addition wikiPageWikiLink Vinylogy.
- Nucleophilic_conjugate_addition wikiPageWikiLink File:(R)-3-phenyl-cyclohanone.png.
- Nucleophilic_conjugate_addition wikiPageWikiLink File:Conjugateadditionexample.png.
- Nucleophilic_conjugate_addition wikiPageWikiLink File:ConjugatedAdditionofThiols.svg.
- Nucleophilic_conjugate_addition wikiPageWikiLink File:EnantioselectiveOrganoCascadeCatalysis.svg.
- Nucleophilic_conjugate_addition wikiPageWikiLink File:NucleophilicConjugateAddition.svg.
- Nucleophilic_conjugate_addition wikiPageWikiLinkText "1,4-addition".
- Nucleophilic_conjugate_addition wikiPageWikiLinkText "1,4-selectivity".
- Nucleophilic_conjugate_addition wikiPageWikiLinkText "Conjugate addition".
- Nucleophilic_conjugate_addition wikiPageWikiLinkText "Michael acceptor".
- Nucleophilic_conjugate_addition wikiPageWikiLinkText "Nucleophilic conjugate addition".
- Nucleophilic_conjugate_addition wikiPageWikiLinkText "conjugate addition".
- Nucleophilic_conjugate_addition wikiPageWikiLinkText "conjugate additions".
- Nucleophilic_conjugate_addition wikiPageWikiLinkText "nucleophilic 1,4-addition".