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- Corey–Kim_oxidation abstract "The Corey–Kim oxidation is an oxidation reaction used to synthesise aldehydes and ketones from primary and secondary alcohols. It is named for American chemist and Nobel Laureate Elias James Corey and Korean-American chemist Choung Un Kim.Although the Corey–Kim oxidation possesses the distinctive advantage over Swern oxidation of allowing an operation above –25 °C, it is not so commonly used due to issues with selectivity in substrates susceptible to chlorination by N-chlorosuccinimide.".
- Corey–Kim_oxidation thumbnail Corey-Kim_Oxidation_Scheme.png?width=300.
- Corey–Kim_oxidation wikiPageExternalLink corey-kim-oxidation.shtm.
- Corey–Kim_oxidation wikiPageID "3764317".
- Corey–Kim_oxidation wikiPageLength "4543".
- Corey–Kim_oxidation wikiPageOutDegree "21".
- Corey–Kim_oxidation wikiPageRevisionID "697883491".
- Corey–Kim_oxidation wikiPageWikiLink Alcohol.
- Corey–Kim_oxidation wikiPageWikiLink Aldehyde.
- Corey–Kim_oxidation wikiPageWikiLink Allyl.
- Corey–Kim_oxidation wikiPageWikiLink Benzyl.
- Corey–Kim_oxidation wikiPageWikiLink Category:Name_reactions.
- Corey–Kim_oxidation wikiPageWikiLink Category:Organic_redox_reactions.
- Corey–Kim_oxidation wikiPageWikiLink Choung_Un_Kim.
- Corey–Kim_oxidation wikiPageWikiLink Dimethyl_sulfide.
- Corey–Kim_oxidation wikiPageWikiLink Elias_James_Corey.
- Corey–Kim_oxidation wikiPageWikiLink Ketone.
- Corey–Kim_oxidation wikiPageWikiLink N-Chlorosuccinimide.
- Corey–Kim_oxidation wikiPageWikiLink Organic_redox_reaction.
- Corey–Kim_oxidation wikiPageWikiLink Pfitzner–Moffatt_oxidation.
- Corey–Kim_oxidation wikiPageWikiLink Swern_oxidation.
- Corey–Kim_oxidation wikiPageWikiLink Triethylamine.
- Corey–Kim_oxidation wikiPageWikiLink File:Corey-Kim_Oxidation_Scheme.png.
- Corey–Kim_oxidation wikiPageWikiLink File:Corey-Kim_oxidation_mechanism.svg.
- Corey–Kim_oxidation wikiPageWikiLinkText "Corey–Kim oxidation".
- Corey–Kim_oxidation wikiPageWikiLinkText "Corey–Kim oxidation".
- Corey–Kim_oxidation name "Corey-Kim oxidation".
- Corey–Kim_oxidation namedafter Elias_James_Corey.
- Corey–Kim_oxidation namedafter "Choung Un Kim".
- Corey–Kim_oxidation type "Organic redox reaction".
- Corey–Kim_oxidation wikiPageUsesTemplate Template:Reactionbox.
- Corey–Kim_oxidation wikiPageUsesTemplate Template:Reactionbox_Identifiers.
- Corey–Kim_oxidation wikiPageUsesTemplate Template:Reflist.
- Corey–Kim_oxidation subject Category:Name_reactions.
- Corey–Kim_oxidation subject Category:Organic_redox_reactions.
- Corey–Kim_oxidation hypernym Reaction.
- Corey–Kim_oxidation type Disease.
- Corey–Kim_oxidation type Eponym.
- Corey–Kim_oxidation type Reaction.
- Corey–Kim_oxidation type Redirect.
- Corey–Kim_oxidation comment "The Corey–Kim oxidation is an oxidation reaction used to synthesise aldehydes and ketones from primary and secondary alcohols. It is named for American chemist and Nobel Laureate Elias James Corey and Korean-American chemist Choung Un Kim.Although the Corey–Kim oxidation possesses the distinctive advantage over Swern oxidation of allowing an operation above –25 °C, it is not so commonly used due to issues with selectivity in substrates susceptible to chlorination by N-chlorosuccinimide.".
- Corey–Kim_oxidation label "Corey–Kim oxidation".
- Corey–Kim_oxidation sameAs Q2316535.
- Corey–Kim_oxidation sameAs Corey-Kim-Oxidation.
- Corey–Kim_oxidation sameAs اکسایش_کوری–کیم.
- Corey–Kim_oxidation sameAs Oxydation_de_Corey-Kim.
- Corey–Kim_oxidation sameAs Oksidasi_Corey-Kim.
- Corey–Kim_oxidation sameAs コーリー・キム酸化.
- Corey–Kim_oxidation sameAs Corey-Kim_산화반응.
- Corey–Kim_oxidation sameAs Corey-Kim-oxidatie.
- Corey–Kim_oxidation sameAs m.09zr8j.
- Corey–Kim_oxidation sameAs Окиснення_за_Корі_—_Кімом.
- Corey–Kim_oxidation sameAs Q2316535.
- Corey–Kim_oxidation sameAs Corey–Kim氧化反应.
- Corey–Kim_oxidation wasDerivedFrom Corey–Kim_oxidation?oldid=697883491.
- Corey–Kim_oxidation depiction Corey-Kim_Oxidation_Scheme.png.
- Corey–Kim_oxidation isPrimaryTopicOf Corey–Kim_oxidation.