Intermolecular, redox-neutral azidoarylation of alkenes via photoredox catalysis was written by Chen, Jian;Zhu, Shengqing;Qin, Jian;Chu, Lingling. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2019.Computed Properties of C6H3FN2 This article mentions the following:
An intermol., redox-neutral azidoarylation of alkenes with pyridines and TMSN3 was reported via visible light-induced photoredox catalysis. This protocol utilized a radical addition/radical coupling sequence, allowing for facile and regioselective installation of versatile β-azido pyridines under redox-neutral and mild conditions. In the experiment, the researchers used many compounds, for example, 2-Fluoroisonicotinonitrile (cas: 3939-14-8Computed Properties of C6H3FN2).
2-Fluoroisonicotinonitrile (cas: 3939-14-8) belongs to pyridine derivatives. The pyridine ring occurs in many important compounds, including agrochemicals, pharmaceuticals, and vitamins. One of the examples of pyridines is the well-known alkaloid lithoprimidine, which is an A3 adenosine receptor antagonist and N,N-dimethylaminopyridine (DMAP) analog, commonly used in organic synthesis.Computed Properties of C6H3FN2