Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/98290
Title: Access to quinolines through gold-catalyzed intermolecular cycloaddition of 2-aminoaryl carbonyls and internal alkynes
Authors: Cai, Shuting
Zeng, Jing
Bai, Yaguang
Liu, Xue-Wei
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
http://hdl.handle.net/10220/17051
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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