26958-75-8Relevant academic research and scientific papers
Unusual reactivity of 2,3-diphenylcyclopropenone towards N-imidoylthioureas; facile synthesis of 3-aryl-2,5,6-triphenylpyrimidin-4(3H)- one (PART III)
Aly, Ashraf A.,NourEl-Din, Ahmed M.,Gomaa, Moshen A.-M.,Brown, Alan B.,Fahmi, Magda S.
, p. 439 - 441 (2008/09/21)
2,3-Diphenylcyclopropenone (1) reacts with N-imidoylthioureas 2a-e to form the pyrimidin-4(3H)-ones 5a-e. The reaction mechanism can be described as due to stepwise addition accompanied by elimination of phenyl isothiocyanate.
SYNTHESIS OF 3-SUBSTITUTED 5,6-DIPHENYLPYRIMIDIN-4-ONES FROM DIPHENYLCYCLOPROPENONE AND N-SUBSTITUTED AMIDE OXIMES
Takahashi, Masahiko,Nogami, Takayuki,Nidaira, Ken-ichi
, p. 581 - 584 (2007/10/02)
3-Substituted 5,6-diphenylpyrimidin-4-ones were prepared regioselectively from diphenylcyclopropenone and N-substituted amide oximes.
