1373436-73-7Relevant academic research and scientific papers
Palladium-catalyzed intermolecular C(sp3)-H amidation
Iglesias, Alvaro,Alvarez, Rosana,De-Lera, Angel R.,Muniz, Kilian
, p. 2225 - 2228 (2012)
Dual capacity: A new palladium-catalyzed intermolecular sequence consisting of the C-H activation and amidation of methyl groups relies on N-fluorobis(phenylsulfonyl)imide (NFSI) as both the oxidant and the nitrogen source. The reaction provides the corresponding arylamines as bissulfonimides along with HF as the only by-product. Both experimental and computational results suggest the involvement of a monomeric palladium(IV) intermediate. Copyright
Copper-catalyzed intermolecular amidation of 8-methylquinolines with: N -fluoroarylsulfonimides via Csp3-H activation
Zhang, Xiaolei,Wu, Rui,Liu, Wanyi,Qian, Dang-Wei,Yang, Jinhui,Jiang, Pengju,Zheng, Qing-Zhong
supporting information, p. 4789 - 4793 (2016/06/13)
An efficient copper-catalyzed C-H amidation of 8-methylquinolines with N-fluoroarylsulfonimides via Csp3-H activation is described. The reaction proceeds with high functional group tolerance, providing a novel approach to valuable quinolin-8-yl
