24743-62-2Relevant academic research and scientific papers
Pyridine-Catalysed Desulfonylative Addition of β-Diketones to Arylazosulfones via Diaziridine Rearrangement
Ji, Xin,Meng, Ling-Guo,Xu, Hailong,Wang, Lei
supporting information, p. 1142 - 1146 (2020/12/31)
A pyridine-catalysed desulfonylative addition of β-diketones to arylazosulfones was developed to obtain diazenyl β-dicarbonyl compounds. The aryldiazenyl group was observed in the desired product from arylazosulfones, and this diazenylation reaction was achieved via a possible rearrangement process based on diaziridine ring cleavage. The scope of the protocol was investigated and a plausible mechanism was given. (Figure presented.).
SYNTHESIS OF PYRIDINE-2(1H)-THIONE AND THIENOPYRIDINE DERIVATIVES
Elgemeie, Galal E. H.,Alnaimi, Ibrahim S.,Alarab, Hafsa F.
, p. 1721 - 1728 (2007/10/02)
A synthesis of pyridine-2(1H)-thiones and thienopyridines utilizing cyanothioacetamide and 2-arylhydrazono-1,3-diphenylpropane-1,3-diones as starting components is described.
