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|Title:||Access to quinolines through gold-catalyzed intermolecular cycloaddition of 2-aminoaryl carbonyls and internal alkynes||Authors:||Cai, Shuting
|Issue Date:||2011||Source:||Cai, S., Zeng, J., Bai, Y., & Liu, X.- W. (2012). Access to Quinolines through Gold-Catalyzed Intermolecular Cycloaddition of 2-Aminoaryl Carbonyls and Internal Alkynes. The Journal of Organic Chemistry, 77(1), 801-807.||Series/Report no.:||The journal of organic chemistry||Abstract:||A facile and general method leading to polyfunctionalized quinolines was developed. In the presence of a highly efficient combination encompassing (PPh)3AuCl and AgOTf, the reactions between 2-aminocarbonyls and an array of internal alkynes proceeded smoothly to afford quinoline derivatives in good to excellent yields (up to 93%).||URI:||https://hdl.handle.net/10356/98290
|DOI:||http://dx.doi.org/10.1021/jo202281x||Rights:||© 2011 American Chemical Society||Fulltext Permission:||none||Fulltext Availability:||No Fulltext|
|Appears in Collections:||SPMS Journal Articles|
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