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dc.contributor.author김원석*
dc.contributor.author권용주*
dc.date.accessioned2023-10-23T16:30:47Z-
dc.date.available2023-10-23T16:30:47Z-
dc.date.issued2023*
dc.identifier.issn2532-2964*
dc.identifier.otherOAK-34077*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/266446-
dc.description.abstractThe ortho-selective alkynylation of polyhalo-substituted (hetero)aryl tosylates was investigated using an integrated continuous-flow/batch protocol. Without the elimination of the tosyloxy group, the regioselective ortho-metalation of the (hetero)aryl tosylates employing n-BuLi and ZnCl2 was successfully achieved in continuous-flow chemistry within 10.92 s (residence time). The Pd-catalyzed Negishi alkynylations of various iodoethynyl (hetero)arenes and the resulting arylzinc species proceeded at room temperature in yields ranging from 51% to 95%. Finally, the synthetic utility of this strategy was validated by the synthesis of benzofuran and pyridofuran derivatives. © 2023 Korean Chemical Society, Seoul & Wiley-VCH GmbH.*
dc.languageEnglish*
dc.publisherJohn Wiley and Sons Inc*
dc.subjectalkynylation*
dc.subjectflow chemistry*
dc.subjectNegishi coupling*
dc.subjectregioselectivity*
dc.subjectzincation*
dc.titleIntegrated continuous-flow/batch protocol for ortho-selective alkynylation of (hetero)aryl tosylates*
dc.typeArticle*
dc.relation.issue9*
dc.relation.volume44*
dc.relation.indexSCOPUS*
dc.relation.startpage772*
dc.relation.lastpage776*
dc.relation.journaltitleBulletin of the Korean Chemical Society*
dc.identifier.doi10.1002/bkcs.12717*
dc.identifier.scopusid2-s2.0-85159342701*
dc.author.googleJu E.-H.*
dc.author.googleLee M.-J.*
dc.author.googleSong J.*
dc.author.googleKwon Y.-J.*
dc.author.googleKim W.-S.*
dc.contributor.scopusid김원석(57203484044)*
dc.contributor.scopusid권용주(57192714799)*
dc.date.modifydate20240318130702*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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