El Ashry, E. S. H. published the artcileScope of reactions of hydrazines and hydrazones. Part X. Bis(aroylhydrazones) and phenylacetylhydrazones of vic-dicarbonyl compounds and their oxidation to 1,2,3-triazoles, Application In Synthesis of 39115-95-2, the publication is Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry (1980), 19B(7), 612-15, database is CAplus.
Treating acenaphthenequinone with hydrazines gave 40-70% monohydrazones I (Z = O, R = Ph, o-, m-, p-MeC6H4 m-, p-ClC6H4, p-IC6H4, p-MeOC6H4, p-O2NC6H4, 3-, 4-pyridyl). Oxidative cyclization of I (R = Ph, Z = NNHBz) by Pb(OAc)4 gave triazole II. The (phenylacetyl)hydrazones of benzil and phenylglyoxal were similarly prepared and cyclized to the triazoles.
Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry published new progress about 39115-95-2. 39115-95-2 belongs to iodides-buliding-blocks, auxiliary class Iodide,Hydrazine,Amine,Benzene,Hydrazide,Amide, name is 4-Iodobenzohydrazide, and the molecular formula is C7H7IN2O, Application In Synthesis of 39115-95-2.
Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com