1380490-62-9Relevant academic research and scientific papers
Diversified aminohydantoins from ureas and thioureas tethered to amides
Bepary, Sukumar,Youn, In Kwon,Lim, Hee-Jong,Lee, Ge Hyeong
, p. 2542 - 2548 (2012)
Intramolecular cyclization of thioureas or ureas tethered to amides afforded 2-iminohydantoins and 2-amino-1H-imidazol-4(5H)-ones in very high yields (87-100%) regardless of the substituent (alkyls or aryls). This reaction proceeds through carbodiimides a
DPT-mediated synthesis of 2-aminoimidazolidin-4-ones from thioureas tethered to amides
Bepary, Sukumar,Youn, In Kwon,Lim, Hee-Jong,Lee, Ge Hyeong
supporting information, p. 1876 - 1880 (2014/07/07)
2-Aminoimidazolidin-4-ones have been synthesized by using di-2-pyridyl thiocarbonate (DPT), taking the thioureas tethered to amides as the starting materials. Both the primary amides and secondary amides have been subjected to this cyclization method and
