1046789-41-6Relevant articles and documents
Ni-Catalyzed C-H Cyanation of (Hetero)arenes with 2-Cyanoisothiazolidine 1,1-Dioxide as a Cyanation Reagent
Ma, Junjie,Liu, Hao,He, Xin,Chen, Zhicheng,Liu, Yue,Hou, Chuanfu,Sun, Zhizhong,Chu, Wenyi
supporting information, p. 2868 - 2872 (2021/05/05)
A nickel-catalyzed C-H cyanation reaction of arenes has been developed using 2-cyanoisothiazolidine 1,1-dioxide as an electrophilic cyanation reagent. Many different directing groups can be used in this cyanation to obtain a series of cyanation products with good yields. Adopting this strategy to introduce a cyano group, natural alkaloid menisporphine was successfully synthesized through cyano group conversion that further proved the practicality of this cyanation method.
Palladium-catalyzed Suzuki-Miyaura coupling of pyridyl-2-boronic esters with aryl halides using highly active and air-stable phosphine chloride and oxide ligands
Yang, David X.,Colletti, Steven L.,Wu, Kevin,Song, Maoying,Li, George Y.,Shen, Hong C.
supporting information; experimental part, p. 381 - 384 (2009/07/11)
(Chemical Equation Presented) The palladium-catalyzed Suzuki-Miyaura coupling of pyridyl-2-boronic esters provided an efficient approach to useful biaryl building blocks containing a 2-pyridyl moiety. The convenient reaction protocol demonstrates its pote
