87489-75-6Relevant academic research and scientific papers
Synthesis of α-aryl esters and nitriles: Deaminative coupling of α-aminoesters and α-aminoacetonitriles with arylboronic acids
Wu, Guojiao,Deng, Yifan,Wu, Chaoqiang,Zhang, Yan,Wang, Jianbo
supporting information, p. 10510 - 10514 (2016/02/18)
Transition-metal-free synthesis of α-aryl esters and nitriles using arylboronic acids with α-aminoesters and α-aminoacetonitriles, respectively, as the starting materials has been developed. The reaction represents a rare case of converting C(sp3)-N bonds into C(sp3)-C(sp2) bonds. The reaction conditions are mild, demonstrate good functional-group tolerance, and can be scaled up. Touch base: A transition-metal-free protocol for the synthesis of α-aryl esters and nitriles by deaminative coupling is presented. Strong bases and transition-metal catalysts are not needed. The new synthetic method uses readily available starting materials and demonstrates wide substrate scope.
A FACILE PREPARATION OF 2-ALKYLINDOLES - POTENTIAL INTERMEDIATES FOR ALKALOIDS
Vedachalam, M.,Mohan, B.,Srinivasan, P.C.
, p. 3531 - 3532 (2007/10/02)
The bromo compound 1 upon alkylation with active methylene compounds followed by the removal of PhS- and PhSO2- groups furnished the title compounds.
