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- Q2316535 subject Q7458901.
- Q2316535 subject Q8703541.
- Q2316535 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.".
- Q2316535 thumbnail Corey-Kim_Oxidation_Scheme.png?width=300.
- Q2316535 wikiPageExternalLink corey-kim-oxidation.shtm.
- Q2316535 wikiPageWikiLink Q101497.
- Q2316535 wikiPageWikiLink Q135171.
- Q2316535 wikiPageWikiLink Q139199.
- Q2316535 wikiPageWikiLink Q156.
- Q2316535 wikiPageWikiLink Q170744.
- Q2316535 wikiPageWikiLink Q2161141.
- Q2316535 wikiPageWikiLink Q286192.
- Q2316535 wikiPageWikiLink Q423133.
- Q2316535 wikiPageWikiLink Q423777.
- Q2316535 wikiPageWikiLink Q7458901.
- Q2316535 wikiPageWikiLink Q818534.
- Q2316535 wikiPageWikiLink Q8703541.
- Q2316535 wikiPageWikiLink Q899430.
- Q2316535 wikiPageWikiLink Q901945.
- Q2316535 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.".
- Q2316535 label "Corey–Kim oxidation".
- Q2316535 depiction Corey-Kim_Oxidation_Scheme.png.