22462-30-2Relevant academic research and scientific papers
Hexafluoroisopropanol-Mediated Redox-Neutral α-C(sp3)-H Functionalization of Cyclic Amines via Hydride Transfer
Shen, Yao-Bin,Wang, Lin-Xuan,Sun, Yun-Ming,Dong, Feng-Ying,Yu, Liping,Liu, Qing,Xiao, Jian
, p. 1915 - 1926 (2020)
Hexafluoroisopropanol has been demonstrated as the versatile promoter for redox-neutral α-C(sp3)-H functionalization of cyclic amines via the cascade [1,5]-hydride transfer/cyclization strategy. A wide range of cyclic amines are functionalized
Facile formation of cyclic aminals through a Br?nsted acid-promoted redox process
Zhang, Chen,Murarka, Sandip,Seidel, Daniel
supporting information; experimental part, p. 419 - 422 (2009/04/10)
(Chemical Equation Presented) Cyclic aminals were prepared through a Br?nsted acid-promoted reaction. This redox neutral process involves iminium ion formation, 1,5 H-transfer, followed by ring closure.
