Yang, Qing; Yan, Xiao-Tong; Feng, Cheng-Tao; Chen, De-Xiang; Yan, Zhong-Zhong; Xu, Kun published the artcile< Tandem Strecker/C(sp3)-H amination reactions for the construction of cyanide-functionalized imidazo[1,5-a]pyridines with NH4SCN as a cyanating agent>, Product Details of C7H8BrN, the main research area is azarene arylmethylamine ammonium thiocyanate iodine pentoxide promoter Strecker oxidation; cyano imidazopyridine preparation.
An I2O5 promoted tandem Strecker/C(sp3)-H amination reaction of pyridine-2-carboxaldehydes, benzylamines and NH4SCN was reported. This multicomponent reaction that allowed the single-step construction of biol. important cyano-functionalized imidazo[1,5-a]pyridines with mol. diversity was realized for the first time. Moreover, the use of safe and easy-to-handle NH4SCN as a surrogate cyanating agent made this protocol appealing for potential applications.
Organic Chemistry Frontiers published new progress about Aralkyl amines Role: RCT (Reactant), RACT (Reactant or Reagent). 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Product Details of C7H8BrN.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary