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- Swern_oxidation abstract "The Swern oxidation, named after Daniel Swern, is a chemical reaction whereby a primary or secondary alcohol is oxidized to an aldehyde or ketone using oxalyl chloride, dimethyl sulfoxide (DMSO) and an organic base, such as triethylamine. The reaction is known for its mild character and wide tolerance of functional groups.The by-products are dimethyl sulfide (Me2S), carbon monoxide (CO), carbon dioxide (CO2) and — when triethylamine is used as base — triethylammonium chloride (Et3NHCl). Two of the by-products, dimethyl sulfide and carbon monoxide, are very toxic volatile compounds, so the reaction and the work-up needs to be performed in a fume hood. Dimethyl sulfide is a volatile liquid (B.P. 37 °C) with an extremely unpleasant odour.".
- Swern_oxidation thumbnail Swern_Oxidation_Scheme.png?width=300.
- Swern_oxidation wikiPageExternalLink swern-oxidation.shtm.
- Swern_oxidation wikiPageID "173870".
- Swern_oxidation wikiPageLength "7945".
- Swern_oxidation wikiPageOutDegree "55".
- Swern_oxidation wikiPageRevisionID "681607505".
- Swern_oxidation wikiPageWikiLink Alcohol.
- Swern_oxidation wikiPageWikiLink Aldehyde.
- Swern_oxidation wikiPageWikiLink Bleach.
- Swern_oxidation wikiPageWikiLink Carbodiimide.
- Swern_oxidation wikiPageWikiLink Carbodiimides.
- Swern_oxidation wikiPageWikiLink Carbon_dioxide.
- Swern_oxidation wikiPageWikiLink Carbon_monoxide.
- Swern_oxidation wikiPageWikiLink Category:Name_reactions.
- Swern_oxidation wikiPageWikiLink Category:Organic_redox_reactions.
- Swern_oxidation wikiPageWikiLink Chemical_reaction.
- Swern_oxidation wikiPageWikiLink Corey-Kim_oxidation.
- Swern_oxidation wikiPageWikiLink Corey–Kim_oxidation.
- Swern_oxidation wikiPageWikiLink Cyanuric_chloride.
- Swern_oxidation wikiPageWikiLink Daniel_Swern.
- Swern_oxidation wikiPageWikiLink Dehydration.
- Swern_oxidation wikiPageWikiLink Deprotonation.
- Swern_oxidation wikiPageWikiLink Dess–Martin_periodinane.
- Swern_oxidation wikiPageWikiLink Diisopropylethylamine.
- Swern_oxidation wikiPageWikiLink Dimethyl_sulfide.
- Swern_oxidation wikiPageWikiLink Dimethyl_sulfoxide.
- Swern_oxidation wikiPageWikiLink Functional_group.
- Swern_oxidation wikiPageWikiLink Jones_oxidation.
- Swern_oxidation wikiPageWikiLink Ketone.
- Swern_oxidation wikiPageWikiLink N,N-Diisopropylethylamine.
- Swern_oxidation wikiPageWikiLink N-Chlorosuccinimide.
- Swern_oxidation wikiPageWikiLink Oxalyl_chloride.
- Swern_oxidation wikiPageWikiLink Parikh-Doering_oxidation.
- Swern_oxidation wikiPageWikiLink Parikh–Doering_oxidation.
- Swern_oxidation wikiPageWikiLink Pfitzner–Moffatt_oxidation.
- Swern_oxidation wikiPageWikiLink Rearrangement_reaction.
- Swern_oxidation wikiPageWikiLink Redox.
- Swern_oxidation wikiPageWikiLink Resonance_(chemistry).
- Swern_oxidation wikiPageWikiLink Sesquiterpene.
- Swern_oxidation wikiPageWikiLink Sodium_hypochlorite.
- Swern_oxidation wikiPageWikiLink Transition_state.
- Swern_oxidation wikiPageWikiLink Triethylamine.
- Swern_oxidation wikiPageWikiLink Triethylammonium_chloride.
- Swern_oxidation wikiPageWikiLink Trifluoroacetic_anhydride.
- Swern_oxidation wikiPageWikiLink Ylide.
- Swern_oxidation wikiPageWikiLink File:Dimethylchlorosulfonium_Formation_Mechanism.png.
- Swern_oxidation wikiPageWikiLink File:IsovelleralPreparationViaSwernOxidation.png.
- Swern_oxidation wikiPageWikiLink File:Swern_Oxidation_Mechanism.png.
- Swern_oxidation wikiPageWikiLink File:Swern_Oxidation_Scheme.png.
- Swern_oxidation wikiPageWikiLinkText "Moffatt–Swern".
- Swern_oxidation wikiPageWikiLinkText "Swern condition".
- Swern_oxidation wikiPageWikiLinkText "Swern oxidation".
- Swern_oxidation wikiPageWikiLinkText "Swern".
- Swern_oxidation hasPhotoCollection Swern_oxidation.
- Swern_oxidation name "Swern oxidation".
- Swern_oxidation namedafter Daniel_Swern.
- Swern_oxidation type "Organic redox reaction".
- Swern_oxidation wikiPageUsesTemplate Template:Reactionbox.
- Swern_oxidation wikiPageUsesTemplate Template:Reflist.
- Swern_oxidation subject Category:Name_reactions.
- Swern_oxidation subject Category:Organic_redox_reactions.
- Swern_oxidation hypernym Reaction.
- Swern_oxidation type Article.
- Swern_oxidation type Disease.
- Swern_oxidation type Article.
- Swern_oxidation type Eponym.
- Swern_oxidation type Reaction.
- Swern_oxidation comment "The Swern oxidation, named after Daniel Swern, is a chemical reaction whereby a primary or secondary alcohol is oxidized to an aldehyde or ketone using oxalyl chloride, dimethyl sulfoxide (DMSO) and an organic base, such as triethylamine. The reaction is known for its mild character and wide tolerance of functional groups.The by-products are dimethyl sulfide (Me2S), carbon monoxide (CO), carbon dioxide (CO2) and — when triethylamine is used as base — triethylammonium chloride (Et3NHCl).".
- Swern_oxidation label "Swern oxidation".
- Swern_oxidation sameAs Category:Swern_oxidation.
- Swern_oxidation sameAs Swern-Oxidation.
- Swern_oxidation sameAs Oxidación_de_Swern.
- Swern_oxidation sameAs Swern-hapetus.
- Swern_oxidation sameAs Oxydation_de_Swern.
- Swern_oxidation sameAs Ossidazione_di_Swern.
- Swern_oxidation sameAs スワーン酸化.
- Swern_oxidation sameAs Swern_산화반응.
- Swern_oxidation sameAs Swern-oxidatie.
- Swern_oxidation sameAs Oxidação_de_Swern.
- Swern_oxidation sameAs m.017g9s.
- Swern_oxidation sameAs Окиснення_за_Сверном.
- Swern_oxidation sameAs Q899430.
- Swern_oxidation sameAs Q899430.
- Swern_oxidation sameAs 斯文氧化反应.
- Swern_oxidation wasDerivedFrom Swern_oxidation?oldid=681607505.
- Swern_oxidation depiction Swern_Oxidation_Scheme.png.
- Swern_oxidation isPrimaryTopicOf Swern_oxidation.