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- Benzoin_condensation abstract "The benzoin condensation is a reaction (often called a condensation reaction, for historical reasons) between two aromatic aldehydes, particularly benzaldehyde. The reaction is catalyzed by a nucleophile such as the cyanide anion or an N-heterocyclic carbene. The reaction product is an aromatic acyloin with benzoin as the parent compound. An early version of the reaction was developed in 1832 by Justus von Liebig and Friedrich Woehler during their research on bitter almond oil. The catalytic version of the reaction was developed by Nikolay Zinin in the late 1830s, and the reaction mechanism for this organic reaction was proposed in 1903 by A. J. Lapworth.".
- Benzoin_condensation thumbnail Benzoin_mechanism.png?width=300.
- Benzoin_condensation wikiPageExternalLink File:Benz_A_startAnimGif.gif.
- Benzoin_condensation wikiPageID "1968182".
- Benzoin_condensation wikiPageLength "5705".
- Benzoin_condensation wikiPageOutDegree "49".
- Benzoin_condensation wikiPageRevisionID "678362761".
- Benzoin_condensation wikiPageWikiLink 1,8-Diazabicycloundec-7-ene.
- Benzoin_condensation wikiPageWikiLink Acyloin.
- Benzoin_condensation wikiPageWikiLink Acyloin_condensation.
- Benzoin_condensation wikiPageWikiLink Aldehyde.
- Benzoin_condensation wikiPageWikiLink Aldol_condensation.
- Benzoin_condensation wikiPageWikiLink Aliphatic_compound.
- Benzoin_condensation wikiPageWikiLink Almond.
- Benzoin_condensation wikiPageWikiLink Aromaticity.
- Benzoin_condensation wikiPageWikiLink Arthur_Lapworth.
- Benzoin_condensation wikiPageWikiLink Base_(chemistry).
- Benzoin_condensation wikiPageWikiLink Benzaldehyde.
- Benzoin_condensation wikiPageWikiLink Benzoin.
- Benzoin_condensation wikiPageWikiLink Biochemistry.
- Benzoin_condensation wikiPageWikiLink Carbonyl.
- Benzoin_condensation wikiPageWikiLink Catalysis.
- Benzoin_condensation wikiPageWikiLink Category:Condensation_reactions.
- Benzoin_condensation wikiPageWikiLink Cofactor_(biochemistry).
- Benzoin_condensation wikiPageWikiLink Condensation_reaction.
- Benzoin_condensation wikiPageWikiLink Cyanide.
- Benzoin_condensation wikiPageWikiLink Deprotonation.
- Benzoin_condensation wikiPageWikiLink Dimer_(chemistry).
- Benzoin_condensation wikiPageWikiLink Enantiomer.
- Benzoin_condensation wikiPageWikiLink Enone.
- Benzoin_condensation wikiPageWikiLink Friedrich_Wöhler.
- Benzoin_condensation wikiPageWikiLink Heterocyclic_compound.
- Benzoin_condensation wikiPageWikiLink Hydrogen_ion.
- Benzoin_condensation wikiPageWikiLink Intramolecular_reaction.
- Benzoin_condensation wikiPageWikiLink Ion.
- Benzoin_condensation wikiPageWikiLink Justus_von_Liebig.
- Benzoin_condensation wikiPageWikiLink Leaving_group.
- Benzoin_condensation wikiPageWikiLink Methyl_vinyl_ketone.
- Benzoin_condensation wikiPageWikiLink Nikolay_Zinin.
- Benzoin_condensation wikiPageWikiLink Nucleophile.
- Benzoin_condensation wikiPageWikiLink Nucleophilic_addition.
- Benzoin_condensation wikiPageWikiLink Organic_reaction.
- Benzoin_condensation wikiPageWikiLink Persistent_carbene.
- Benzoin_condensation wikiPageWikiLink Potassium_tert-butoxide.
- Benzoin_condensation wikiPageWikiLink Reaction_mechanism.
- Benzoin_condensation wikiPageWikiLink Reversible_reaction.
- Benzoin_condensation wikiPageWikiLink Sodium_cyanide.
- Benzoin_condensation wikiPageWikiLink Stetter_reaction.
- Benzoin_condensation wikiPageWikiLink Thiamine.
- Benzoin_condensation wikiPageWikiLink Thiazole.
- Benzoin_condensation wikiPageWikiLink Umpolung.
- Benzoin_condensation wikiPageWikiLink File:Benzoin_mechanism.png.
- Benzoin_condensation wikiPageWikiLink File:Intramolecularbenzoin.png.
- Benzoin_condensation wikiPageWikiLink File:Intramolecularbenzoin_Takikawa2.png.
- Benzoin_condensation wikiPageWikiLinkText "Benzoin condensation".
- Benzoin_condensation wikiPageWikiLinkText "benzoin condensation".
- Benzoin_condensation subject Category:Condensation_reactions.
- Benzoin_condensation hypernym Reaction.
- Benzoin_condensation type Disease.
- Benzoin_condensation type Reaction.
- Benzoin_condensation comment "The benzoin condensation is a reaction (often called a condensation reaction, for historical reasons) between two aromatic aldehydes, particularly benzaldehyde. The reaction is catalyzed by a nucleophile such as the cyanide anion or an N-heterocyclic carbene. The reaction product is an aromatic acyloin with benzoin as the parent compound. An early version of the reaction was developed in 1832 by Justus von Liebig and Friedrich Woehler during their research on bitter almond oil.".
- Benzoin_condensation label "Benzoin condensation".
- Benzoin_condensation sameAs Q818514.
- Benzoin_condensation sameAs Benzoin-Addition.
- Benzoin_condensation sameAs Condensación_benzoínica.
- Benzoin_condensation sameAs Bensoiinkondensatsioon.
- Benzoin_condensation sameAs Bentsoiinikondensaatio.
- Benzoin_condensation sameAs Condensazione_benzoinica.
- Benzoin_condensation sameAs ベンゾイン縮合.
- Benzoin_condensation sameAs Benzoïnecondensatie.
- Benzoin_condensation sameAs m.069r8_.
- Benzoin_condensation sameAs Q818514.
- Benzoin_condensation sameAs 安息香缩合反应.
- Benzoin_condensation wasDerivedFrom Benzoin_condensation?oldid=678362761.
- Benzoin_condensation depiction Benzoin_mechanism.png.
- Benzoin_condensation isPrimaryTopicOf Benzoin_condensation.