99224-30-3Relevant articles and documents
Asymmetric construction of quaternary α-nitro amides by palladium-catalyzed C(sp3)-H arylation
Kong, Wei-Xin,Xie, Shi-Jing,Cao, Chen-Yao-Zi,Zhang, Chao-Wei,Wang, Chuanyong,Duan, Wei-Liang
, p. 2292 - 2295 (2020)
Pd-Catalyzed enantioselective C(sp3)-H arylation of N-(o-Br-aryl) anilides has been disclosed, and quaternary α-nitro amides were constructed with up to 98% ee. The presence of the nitro group on the substrate enables the progress of the reaction and the ready transformation of the product to optically active quaternary amino acid derivatives.