Rudenko, A. P. et al. published their research in Zhurnal Organicheskoi Khimii in 1984 | CAS: 16144-65-3

2,2′,2”-(2,4,6-Trimethylbenzene-1,3,5-triyl)triacetonitrile (cas: 16144-65-3) belongs to nitriles. Nitrile compounds can be prepared by the incorporation of a cyanide source through C–C bond formation or by dehydration of primary carboxamides. Asymmetric bioreduction of nitriles is an attractive route to produce optically active nitriles as current metal-catalyzed hydrogenations tend to have low reactivity.Category: nitriles-buliding-blocks

Electrochemical oxidation of organic compounds in fluorosulfuric acid. VIII. Current-voltage characteristics of the oxidation of aromatic compounds in fluorosulfuric acid and acetonitrile was written by Rudenko, A. P.;Zarubin, M. Ya.;Pragst, Fritz. And the article was included in Zhurnal Organicheskoi Khimii in 1984.Category: nitriles-buliding-blocks The following contents are mentioned in the article:

Cyclic voltammograms were obtained for the oxidation of polysubstituted benzenes and diphenylmethanes containing electron-withdrawing groups (e.g., SO2F, NO2, CN, CO2H) in HSO3F and MeCN. In most cases the oxidation in HSO3F leads reversibly to the cation radical at low rates of potential scanning; in MeCN the process is irreversible even at high scanning rates (up to 100 V/s). This study involved multiple reactions and reactants, such as 2,2′,2”-(2,4,6-Trimethylbenzene-1,3,5-triyl)triacetonitrile (cas: 16144-65-3Category: nitriles-buliding-blocks).

2,2′,2”-(2,4,6-Trimethylbenzene-1,3,5-triyl)triacetonitrile (cas: 16144-65-3) belongs to nitriles. Nitrile compounds can be prepared by the incorporation of a cyanide source through C–C bond formation or by dehydration of primary carboxamides. Asymmetric bioreduction of nitriles is an attractive route to produce optically active nitriles as current metal-catalyzed hydrogenations tend to have low reactivity.Category: nitriles-buliding-blocks

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts