1158968-93-4Relevant academic research and scientific papers
Iodocyclization of n-arylpropynamides mediated by hypervalent iodine reagent: Divergent synthesis of iodinated quinolin-2-ones and spiro[4,5]trienones
Zhou, Ying,Zhang, Xiang,Zhang, Yong,Ruan, Linxin,Zhang, Jiacheng,Zhang-Negrerie, Daisy,Du, Yunfei
supporting information, p. 150 - 153 (2017/11/27)
PhI(OCOCF3)2 acts as both a nonmetal oxidant and an iodination reagent to trigger iodocyclization of N-arylpropynamides while selectively affording iodinated quinolin-2-ones or the spiro[4,5]trienone skeleton, depending on the substituent pattern. In cases where the Narylpropynamide bears a para-fluorine on the aniline ring, the spiro compound is formed via an exclusive defluorination process; otherwise, the product was quinolin-2-one.
Copper-catalyzed difunctionalization of activated alkynes by radical oxidation-tandem cyclization/dearomatization to synthesize 3-trifluoromethyl spiro[4.5]trienones
Hua, Hui-Liang,He, Yu-Tao,Qiu, Yi-Feng,Li, Ying-Xiu,Song, Bo,Gao, Pin,Song, Xian-Rong,Guo, Dong-Hui,Liu, Xue-Yuan,Liang, Yong-Min
supporting information, p. 1468 - 1473 (2015/01/30)
A copper-catalyzed difunctionalizing trifluoromethylation of activated alkynes with the cheap reagent sodium trifluoromethanesulfinate (NaSO2CF3 or Langlois' reagent) has been developed incorporating a tandem cyclization/ dearomatiza
