73710-98-2Relevant academic research and scientific papers
Construction of sequence-defined polytriazoles by IrAAC and CuAAC reactions
Ding, Shengtao,Ju, Changhong,Ma, Jiahao,Meng, Congcong,Zhang, Xueyan
supporting information, p. 3955 - 3958 (2020/04/17)
Here we report the first synthesis of sequence-defined polytriazoles, in which different side groups are sequentially anchored to the C-5 position of 1,2,3-triazole rings. By using efficient synthetic strategies based on IrAAC and CuAAC, different monodis
Highly regioselective hydrosilylation of unsymmetric alkynes using a phenylthio directing group
Huang, Kuan-Hsun,Isobe, Minoru
supporting information, p. 4733 - 4740 (2014/08/05)
Cobalt-assisted hydrosilylation of acetylenes is particularly interesting in organic synthesis since alkynyl group functionalization can give way to more useful substructures. This study aims to answer the general question of how to control hydrosilylatio
Iridium-catalyzed intermolecular azide-alkyne cycloaddition of internal thioalkynes under mild conditions
Ding, Shengtao,Jia, Guochen,Sun, Jianwei
supporting information, p. 1877 - 1880 (2014/03/21)
An iridium-catalyzed azide-alkyne cycloaddition reaction (IrAAC) of electron-rich internal alkynes is described. It is the first efficient intermolecular AAC of internal thioalkynes. The reaction exhibits remarkable features, such as high efficiency and r
Short and efficient preparation of alkynyl selenides, sulfides and tellurides from terminal alkynes
Bieber, Lothar W.,Da Silva, Margarete F.,Menezes, Paulo H.
, p. 2735 - 2737 (2007/10/03)
Diphenyl diselenide reacts with terminal alkynes at room temperature in DMSO in the presence of catalytic amounts of copper iodide to give good to excellent yields of alkynyl phenyl selenides. The reaction occurs under neutral conditions and the solvent a
