1443367-97-2Relevant academic research and scientific papers
TEMPO-mediated allylic C-H amination with hydrazones
Zhu, Xu,Chiba, Shunsuke
supporting information, p. 4567 - 4570 (2014/06/24)
TEMPO-mediated reactions of alkenyl hydrazones afforded azaheterocycles via sp3 C-H allylic amination. The transformation is featured by a sequence of remote allylic H-radical shift and allylic homolytic substitution with hydrazone radicals. This journal is
TEMPO-mediated aliphatic C-H Oxidation with Oximes and hydrazones
Zhu, Xu,Wang, Yi-Feng,Ren, Wei,Zhang, Feng-Lian,Chiba, Shunsuke
supporting information, p. 3214 - 3217 (2013/07/26)
A method for aliphatic C-H bond oxidation of oximes and hydrazones mediated by 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) has been developed, which enables the concise assembly of substituted isoxazole and pyrazole skeletons.
