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