1342819-66-2Relevant academic research and scientific papers
Nonafluorobutanesulfonyl azide as a shelf-stable highly reactive oxidant for the copper-catalyzed synthesis of 1,3-diynes from terminal alkynes
Suárez, José Ramón,Collado-Sanz, Daniel,Cárdenas, Diego J.,Chiara, Jose Luis
, p. 1098 - 1106 (2015/01/30)
Nonafluorobutanesulfonyl azide is a highly efficient reagent for the copper-catalyzed coupling of terminal alkynes to give symmetrical and unsymmetrical 1,3-diynes in good to excellent yields and with good functional group compatibility. The reaction is e
Carbon dioxide-mediated synthesis of 3(2H)-furanones from diyne alcohols
Yuan, Gaoqing,He, Zaijun,Zheng, Junhua,Chen, Zhengwang,Huang, Huawen,Shi, Dabin,Qi, Chaorong,Jiang, Huanfeng
supporting information; experimental part, p. 5956 - 5959 (2011/11/28)
A novel type of carbon dioxide-mediated reaction of diyne alcohols without any metal catalysts was reported. Carbon dioxide held the key to the success of this reaction, in which 3(2H)-furanones were selectively obtained in moderate to high yields.
