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dc.contributor.author류재상*
dc.date.accessioned2016-08-27T04:08:57Z-
dc.date.available2016-08-27T04:08:57Z-
dc.date.issued2014*
dc.identifier.issn0253-2964*
dc.identifier.issn1229-5949*
dc.identifier.otherOAK-11891*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/216897-
dc.description.abstractGold-catalyzed tandem cyclization oxidative alkynylation and cyclization-fluorination reactions of 2-alkynone O-methyloximes are described. The reactions proceed smoothly at room temperature in the presence of 10 mol % of (PPh3)AuNTf2, 2.5 equivalents of selectfluor, and 2 equivalents of K3PO4. 2-Alkynone O-methyloximes undergo intramolecular oxyauration/cyclization and ensuing oxidative cross-coupling and fluorination process to afford the corresponding 3,4,5-trisubstituted isoxazoles in a cascade manner.*
dc.languageEnglish*
dc.publisherKOREAN CHEMICAL SOC*
dc.subjectGold*
dc.subjectIsoxazole*
dc.subjectO-Methyloxime*
dc.subjectCross-coupling*
dc.subjectAlkyne*
dc.titleSynthesis of 3,4,5-Trisubstituted Isoxazoles through Gold-Catalyzed Cascade Cyclization Oxidative Alkynylation and Cyclization-Fluorination of 2-Alkynone O-Methyloximes*
dc.typeArticle*
dc.relation.issue9*
dc.relation.volume35*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.indexKCI*
dc.relation.startpage2635*
dc.relation.lastpage2644*
dc.relation.journaltitleBULLETIN OF THE KOREAN CHEMICAL SOCIETY*
dc.identifier.doi10.5012/bkcs.2014.35.9.2635*
dc.identifier.wosidWOS:000342332500007*
dc.identifier.scopusid2-s2.0-84927134583*
dc.author.googleSong, Doo-Hee*
dc.author.googleRyu, Jae-Sang*
dc.contributor.scopusid류재상(36081118200)*
dc.date.modifydate20231120165709*
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약학대학 > 약학과 > Journal papers
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