Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Oppenauer_oxidation> ?p ?o }
- Oppenauer_oxidation abstract "Oppenauer oxidation, named after Rupert Viktor Oppenauer, is a gentle method for selectively oxidizing secondary alcohols to ketones.The reaction is the opposite of Meerwein–Ponndorf–Verley reduction. The alcohol is oxidized with aluminium isopropoxide in excess acetone. This shifts the equilibrium toward the product side.The oxidation is highly selective for secondary alcohols and does not oxidize other sensitive functional groups such as amines and sulfides. Though primary alcohols can be oxidized under Oppenauer conditions, primary alcohols are seldom oxidized by this method due to the competing aldol condensation of aldehyde products. The Oppenauer oxidation is still used for the oxidation of acid labile substrates. The method has been largely displaced by oxidation methods based on chromates (e.g. pyridinium chlorochromate) or dimethyl sulfoxide (e.g. Swern oxidation) or Dess–Martin oxidation due to its use of relatively mild and non-toxic reagents (e.g. the reaction is run in acetone/benzene mixtures). The Oppenanuer oxidation is commonly used in various industrial processes such as the synthesis of steroids, hormones, alkaloids, terpenes, etc.".
- Oppenauer_oxidation thumbnail Oppenauer_oxidation_reaction_scheme.png?width=300.
- Oppenauer_oxidation wikiPageID "6343849".
- Oppenauer_oxidation wikiPageLength "10934".
- Oppenauer_oxidation wikiPageOutDegree "92".
- Oppenauer_oxidation wikiPageRevisionID "697807926".
- Oppenauer_oxidation wikiPageWikiLink 3-Nitrobenzaldehyde.
- Oppenauer_oxidation wikiPageWikiLink Acetone.
- Oppenauer_oxidation wikiPageWikiLink Alcohol.
- Oppenauer_oxidation wikiPageWikiLink Aldehyde.
- Oppenauer_oxidation wikiPageWikiLink Aldol_condensation.
- Oppenauer_oxidation wikiPageWikiLink Alkaloid.
- Oppenauer_oxidation wikiPageWikiLink Alkoxide.
- Oppenauer_oxidation wikiPageWikiLink Allyl_alcohol.
- Oppenauer_oxidation wikiPageWikiLink Aluminium.
- Oppenauer_oxidation wikiPageWikiLink Aluminium_isopropoxide.
- Oppenauer_oxidation wikiPageWikiLink Amine.
- Oppenauer_oxidation wikiPageWikiLink Analgesic.
- Oppenauer_oxidation wikiPageWikiLink Anhydrous.
- Oppenauer_oxidation wikiPageWikiLink Base_(chemistry).
- Oppenauer_oxidation wikiPageWikiLink Benzene.
- Oppenauer_oxidation wikiPageWikiLink Benzophenone.
- Oppenauer_oxidation wikiPageWikiLink Benzoquinone.
- Oppenauer_oxidation wikiPageWikiLink Boris_Tishchenko.
- Oppenauer_oxidation wikiPageWikiLink Borneol.
- Oppenauer_oxidation wikiPageWikiLink Camphor.
- Oppenauer_oxidation wikiPageWikiLink Carbonyl.
- Oppenauer_oxidation wikiPageWikiLink Carboxylic_acid.
- Oppenauer_oxidation wikiPageWikiLink Carveol.
- Oppenauer_oxidation wikiPageWikiLink Carvone.
- Oppenauer_oxidation wikiPageWikiLink Catalysis.
- Oppenauer_oxidation wikiPageWikiLink Category:Name_reactions.
- Oppenauer_oxidation wikiPageWikiLink Category:Organic_redox_reactions.
- Oppenauer_oxidation wikiPageWikiLink Chemical_equilibrium.
- Oppenauer_oxidation wikiPageWikiLink Chemical_reaction.
- Oppenauer_oxidation wikiPageWikiLink Chemoselectivity.
- Oppenauer_oxidation wikiPageWikiLink Chromate_and_dichromate.
- Oppenauer_oxidation wikiPageWikiLink Codeine.
- Oppenauer_oxidation wikiPageWikiLink Codeinone.
- Oppenauer_oxidation wikiPageWikiLink Dess–Martin_periodinane.
- Oppenauer_oxidation wikiPageWikiLink Dimethyl_sulfoxide.
- Oppenauer_oxidation wikiPageWikiLink Diol.
- Oppenauer_oxidation wikiPageWikiLink Hormone.
- Oppenauer_oxidation wikiPageWikiLink Hydride.
- Oppenauer_oxidation wikiPageWikiLink Hydrogen.
- Oppenauer_oxidation wikiPageWikiLink Jones_oxidation.
- Oppenauer_oxidation wikiPageWikiLink Ketone.
- Oppenauer_oxidation wikiPageWikiLink Lactone.
- Oppenauer_oxidation wikiPageWikiLink Meerwein–Ponndorf–Verley_reduction.
- Oppenauer_oxidation wikiPageWikiLink Morphine.
- Oppenauer_oxidation wikiPageWikiLink Nitrogen.
- Oppenauer_oxidation wikiPageWikiLink Organic_redox_reaction.
- Oppenauer_oxidation wikiPageWikiLink Pharmaceutical_industry.
- Oppenauer_oxidation wikiPageWikiLink Potassium_tert-butoxide.
- Oppenauer_oxidation wikiPageWikiLink Pregnenolone.
- Oppenauer_oxidation wikiPageWikiLink Progesterone.
- Oppenauer_oxidation wikiPageWikiLink Pyridinium_chlorochromate.
- Oppenauer_oxidation wikiPageWikiLink Quinine.
- Oppenauer_oxidation wikiPageWikiLink Reaction_intermediate.
- Oppenauer_oxidation wikiPageWikiLink Reaction_mechanism.
- Oppenauer_oxidation wikiPageWikiLink Redox.
- Oppenauer_oxidation wikiPageWikiLink Ruthenium.
- Oppenauer_oxidation wikiPageWikiLink Saturation_(chemistry).
- Oppenauer_oxidation wikiPageWikiLink Steroid.
- Oppenauer_oxidation wikiPageWikiLink Substrate_(chemistry).
- Oppenauer_oxidation wikiPageWikiLink Sulfide.
- Oppenauer_oxidation wikiPageWikiLink Swern_oxidation.
- Oppenauer_oxidation wikiPageWikiLink Terpene.
- Oppenauer_oxidation wikiPageWikiLink Terpenoid.
- Oppenauer_oxidation wikiPageWikiLink Transition_state.
- Oppenauer_oxidation wikiPageWikiLink Trimethylaluminium.
- Oppenauer_oxidation wikiPageWikiLink File:Aldol_condensation.png.
- Oppenauer_oxidation wikiPageWikiLink File:Codeine_syn.png.
- Oppenauer_oxidation wikiPageWikiLink File:Lactone.png.
- Oppenauer_oxidation wikiPageWikiLink File:Oppenauer_oxidation_mechanism_layout.png.
- Oppenauer_oxidation wikiPageWikiLink File:Oppenauer_oxidation_reaction_scheme.png.
- Oppenauer_oxidation wikiPageWikiLink File:Other_modification_1.png.
- Oppenauer_oxidation wikiPageWikiLink File:Other_modification_2.png.
- Oppenauer_oxidation wikiPageWikiLink File:Pregnenolone_syn.png.
- Oppenauer_oxidation wikiPageWikiLink File:Steroid.png.
- Oppenauer_oxidation wikiPageWikiLink File:Wettstein_oppenauer_reaction.png.
- Oppenauer_oxidation wikiPageWikiLink File:Wiki-oppenaure-mxa2.tif.
- Oppenauer_oxidation wikiPageWikiLink File:Woodward_modification.png.
- Oppenauer_oxidation wikiPageWikiLinkText "Oppenauer oxidation".
- Oppenauer_oxidation wikiPageWikiLinkText "Oppenauer reaction".
- Oppenauer_oxidation wikiPageUsesTemplate Template:Reflist.
- Oppenauer_oxidation subject Category:Name_reactions.
- Oppenauer_oxidation subject Category:Organic_redox_reactions.
- Oppenauer_oxidation hypernym Method.
- Oppenauer_oxidation type Software.
- Oppenauer_oxidation type Eponym.
- Oppenauer_oxidation type Reaction.
- Oppenauer_oxidation type Redirect.
- Oppenauer_oxidation comment "Oppenauer oxidation, named after Rupert Viktor Oppenauer, is a gentle method for selectively oxidizing secondary alcohols to ketones.The reaction is the opposite of Meerwein–Ponndorf–Verley reduction. The alcohol is oxidized with aluminium isopropoxide in excess acetone. This shifts the equilibrium toward the product side.The oxidation is highly selective for secondary alcohols and does not oxidize other sensitive functional groups such as amines and sulfides.".
- Oppenauer_oxidation label "Oppenauer oxidation".
- Oppenauer_oxidation sameAs Q902263.
- Oppenauer_oxidation sameAs Oppenauer-Oxidation.
- Oppenauer_oxidation sameAs Oxidación_de_Oppenauer.
- Oppenauer_oxidation sameAs Oxydation_dOppenauer.
- Oppenauer_oxidation sameAs Ossidazione_di_Oppenauer.