Tam Huynh Dinh; Kolb, Annie; Gouyette, Catherine; Igolen, Jean published an article in 1975, the title of the article was Synthesis of C-nucleosides. VII. β-D-Ribofuranosyl-2- and -8-adenines.Application In Synthesis of 2-Aminomalononitrile 4-methylbenzenesulfonate And the article contains the following content:
Benzyl (O-benzoyl-5-D-ribofuranosyl)thioformimidate reacted with aminomalodinitrile or with 5-amino-4-cyanoimidazole to yield the two C-nucleoside analogs I and II of adenosine. The β-configuration was determined with NMR and CD spectra. The experimental process involved the reaction of 2-Aminomalononitrile 4-methylbenzenesulfonate(cas: 5098-14-6).Application In Synthesis of 2-Aminomalononitrile 4-methylbenzenesulfonate
The Article related to ribosylthioformimidate aminomalonitrile cycloaddition, imidazole amino ribosylthioformimidate cycloaddition, adenosine carbon nucleoside, Carbohydrates: Nucleosides, Nucleotides and other aspects.Application In Synthesis of 2-Aminomalononitrile 4-methylbenzenesulfonate
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts