88103-75-7Relevant academic research and scientific papers
Synthesis of Multisubstituted Pyrroles from Enolizable Aldehydes and Primary Amines Promoted by Iodine
Huang, Wenbo,Chen, Shaomin,Chen, Zhiyan,Yue, Meie,Li, Minghao,Gu, Yanlong
, p. 5655 - 5666 (2019/05/10)
1,2,4-Trisubstituted pyrroles were synthesized from enolizable aliphatic aldehydes and primary aliphatic amines by using iodine as the dual Lewis acid/mild oxidant. In the presence of 3.0 equiv of TBHP, enolizable α,β-unsaturated aldehyde, for example, co
A NOVEL PHOTOREARRANGEMENT OF 2,5-DIARYL-1,4-DITHIIN-1,1-DIOXIDE ACCOMPANIED BY EXTRUSION OF SULFUR DIOXIDE
Kobayashi, Keiji,Mutai, Kiyoshi
, p. 1461 - 1462 (2007/10/02)
Photolysis of the title compound afforded 2,5-diarylthiophene.The mechanism involving the valence isomerization to the thioketone was supported by the photolysis in n-butylamine, which gave pyrrole derivatives.
