Efficient synthesis of isoquinolines in water by a Pd-catalyzed tandem reaction of functionalized alkylnitriles with arylboronic acids. Issue 7 (9th March 2017)

• Record Type: Journal Article
• Authors: Hu, Kun; Qi, Linjun; Yu, Shuling; Cheng, Tianxing; Wang, Xiaodong; Li, Zhaojun; Xia, Yuanzhi; Chen, Jiuxi; Wu, Huayue
• Is Part Of: Green chemistry. Volume 19:Issue 7(2017)
• Page Start: 1740
• Page End: 1750
• Publication Date: 2017-03-09
• Subjects: Environmental chemistry -- Industrial applications -- Periodicals; Environmental management -- Periodicals; 660
• DOI: 10.1039/c7gc00267j
• Languages: English
• ISSNs: 1463-9262

Abstract

Abstract : Pd-catalyzed tandem reaction of functionalized alkylnitriles with arylboronic acids for the synthesis of diverse isoquinolines in water. Abstract : A palladium-catalyzed tandem reaction of 2-(cyanomethyl)benzonitriles or 2-(2-carbonylphenyl)acetonitriles with arylboronic acids in water has been developed for the first time. This reaction features good functional group tolerance and provides a new strategy for the synthesis of diverse isoquinolines under mild conditions. The use of water as the reaction medium makes the synthesis process environmentally benign. Preliminary mechanistic experiments indicate that the major reaction pathway involves carbopalladation of the C(sp 3 )–cyano group and subsequent intramolecular cyclization findings that were further supported by density functional theory (DFT) calculations.