82093-41-2Relevant articles and documents
Ring-Opening Reaction of Imidazo[1,2-a]pyridines Using (Diacetoxyiodo)benzene and NaN3: The Synthesis of α-Iminonitriles
Kalbandhe, Amit H.,Kavale, Ashish C.,Karade, Nandkishor N.
, p. 1318 - 1322 (2017)
The reaction of imidazo[1,2-a]pyridine with NaN3 in the presence of (diacetoxyiodo)benzene as an oxidant resulted in the unusual formation of α-iminonitriles in good yields under mild conditions. This method provides access to α-iminonitriles under cyanide-free and metal-free reaction conditions.
Radical ring opening reaction of pyridine fused heterocycles with IBA-N3 catalyzed by tetra-n-butylammonium iodide
Wang, Ruonan,Wang, Shiwei,Li, Dayong,Ye, Feiyang,Leng, Yuting,Wu, Yangjie,Chang, Junbiao,Wu, Yusheng
supporting information, p. 2298 - 2305 (2019/03/13)
A mild, metal-free and efficient synthesis of 2,3-disubstituted acrylonitriles and α-iminonitriles through radical ring opening reaction of pyridine fused heterocycles has been developed. The tetra-n-butylammonium iodide catalyst acts as a formal one-elec
Reaction of 3-Nitroso-2-phenylimidazopyridine with Triethyl Phosphite. A Revised Structure for the Product
Birch, David J.,Guildford, Allen J.,Tometzki, Margaret A.,Turner, Ralph W.
, p. 3547 - 3548 (2007/10/02)
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