17282-90-5Relevant articles and documents
An efficient heterogeneous gold(I)-catalyzed intermolecular cycloaddition of 2-aminoaryl carbonyls and internal alkynes leading to polyfunctionalized quinolines
Hu, Wenli,Yang, Weisen,Yan, Tao,Cai, Mingzhong
supporting information, p. 799 - 813 (2019/03/23)
The first heterogeneous intermolecular cycloaddition of 2-aminoaryl carbonyls and internal alkynes was realized in DMF at 100 °C by using a triphenylphosphine-functionalized MCM-41-supported gold(I) complex [MCM-41-PPh3-AuCl] and AgOTf as catal
Regioselective intramolecular annulations of ambident β-enamino esters: A diversity-oriented synthesis of nitrogen-containing privileged molecules
Yaragorla, Srinivasarao,Pareek, Abhishek
supporting information, p. 909 - 913 (2018/02/12)
Diversity-oriented, regioselective, intramolecular annulation of β-enamino esters is described under solvent-free, calcium-catalysis. 2-aminoaryl ketones and alkyl propiolates undergone a [4+2] annulation to yield substituted quinolines; with an excess of
Palladium-catalyzed synthesis of polysubstituted quinolines from 2-amino aromatic ketones and alkynes
Zhou, Wang,Lei, Jianhua
supporting information, p. 5583 - 5585 (2014/05/20)
A palladium-catalyzed one-pot method for the synthesis of quinolines from commercial or readily available 2-amino aromatic ketones and alkynes is reported for the first time. This transformation offers an alternative method for the synthesis of polysubstituted quinoline. the Partner Organisations 2014.
