27429-70-5Relevant academic research and scientific papers
Synthesis of rutaecarpine alkaloids: Via an electrochemical cross dehydrogenation coupling reaction
Li, Qian-Yu,Cheng, Shi-Yan,Tang, Hai-Tao,Pan, Ying-Ming
, p. 5517 - 5520 (2019)
Substrates are directly oxidized at the anode without using any metal catalyst and oxidant to obtain a series of nitrogen heterocyclic compounds, including benzimidazoles and quinolinones. These compounds are highly tolerant to various functional groups and heterocycle-containing substrates. In addition, natural alkaloids, such as rutaecarpine and deoxyvasicinone, can be synthesized by this method.
