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

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dc.contributor.author	Du, Xiaochen
dc.contributor.author	Huang, Jianjun
dc.contributor.author	Nechaev, Anton A.
dc.contributor.author	Yao, Ruwei
dc.contributor.author	Gong, Jing
dc.contributor.author	Van der Eycken, Erik V.
dc.contributor.author	Pereshivko, Olga P.
dc.contributor.author	Peshkov, Vsevolod A.
dc.date.accessioned	2020-03-31T06:51:12Z
dc.date.available	2020-03-31T06:51:12Z
dc.date.issued	2018-10-04
dc.identifier.citation	Du, X.; Huang, J.; Nechaev, A. A.; Yao, R.; Gong, J.; Van der Eycken, E. V.; Pereshivko, O. P.; Peshkov, V. A. Beilstein J. Org. Chem. 2018, 14, 2572–2579. doi:10.3762/bjoc.14.234	en_US
dc.identifier.uri	http://nur.nu.edu.kz/handle/123456789/4571
dc.description.abstract	A 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_US
dc.language.iso	en	en_US
dc.publisher	Beilstein J. Org. Chem.	en_US
dc.rights	Attribution-NonCommercial-ShareAlike 3.0 United States	*
dc.rights.uri	http://creativecommons.org/licenses/by-nc-sa/3.0/us/	*
dc.subject	gold catalysis	en_US
dc.subject	hydroarylation	en_US
dc.subject	Ugi reaction	en_US
dc.title	Gold-catalyzed post-Ugi alkyne hydroarylation for the synthesis of 2-quinolones	en_US
dc.type	Article	en_US
workflow.import.source	science