Gold-catalyzed post-Ugi alkyne hydroarylation for the synthesis of 2-quinolones

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dc.contributor.authorPeshkov, Vsevolod A
dc.contributor.authorPereshivko, Olga P
dc.contributor.authorVan der Eycken, Erik V
dc.contributor.authorGong, Jing
dc.contributor.authorYao, Ruwei
dc.contributor.authorNechaev, Anton A
dc.contributor.authorHuang, Jianjun
dc.contributor.authorDu, Xiaochen
dc.contributor.authorDu, Xiaochen
dc.date.accessioned2025-08-19T09:25:26Z
dc.date.available2025-08-19T09:25:26Z
dc.date.issued2018-10-04
dc.description.abstractA series of propargylamides containing an electron-rich benzene ring was prepared through the Ugi reaction of 3,5-dimethoxyaniline with various propiolic acids, aldehydes and isocyanides. Subjecting these adducts to a gold-catalyzed intramolecular alkyne hydroarylation process allowed to efficiently construct the 2-quinolone core bearing a branched substituent on the nitrogen atom.en
dc.identifier.doi10.3762/bjoc.14.234
dc.identifier.issn1860-5397
dc.identifier.otherFilename:10.3762_bjoc.14.234.pdf
dc.identifier.urihttps://doi.org/10.3762/bjoc.14.234
dc.identifier.urihttps://nur.nu.edu.kz/handle/123456789/9546
dc.language.isoen
dc.publisherBeilstein Institut
dc.relation.ispartofBeilstein Journal of Organic Chemistryen
dc.sourceBeilstein Journal of Organic Chemistry, 14, 2572-2579, (2018)en
dc.titleGold-catalyzed post-Ugi alkyne hydroarylation for the synthesis of 2-quinolonesen
dc.typeJournal Articleen

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