1253101-13-1Relevant articles and documents
Silver-catalyzed one-pot synthesis of benzyl 2-alkynoates under ambient pressure of CO2and ligand-free conditions
Guo, Fang-Jie,Zhang, Zhi-Zhi,Wang, Jing-Yun,Sun, Jing,Fang, Xiang-Chen,Zhou, Ming-Dong
, p. 900 - 906 (2017/01/28)
The carboxylative coupling of aryl/alkyl terminal alkynes, CO2and benzyl halides was investigated using silver iodide as the catalyst and Cs2CO3as the base in CH3CN under ligand-free conditions. This reaction protocol shows a wide substrate scope and high functional group tolerance ability for benzyl halides, in which various functionalized benzyl 2-alkynoates were achieved in good yields. This one-pot, ligand-free and CH3CN mediated reaction proved to be easy to handle and could be facilitated under atmospheric CO2pressure.
Ligand-free Ag(I)-catalyzed carboxylative coupling of terminal alkynes, chloride compounds, and CO2
Zhang, Xiao,Zhang, Wen-Zhen,Shi, Ling-Long,Zhu, Chuang,Jiang, Jiao-Lai,Lu, Xiao-Bing
, p. 9085 - 9089 (2013/01/13)
Simple silver(I) slats were found to be highly efficient and selective catalyst for carboxylative coupling of aryl- or alkyl-substituted terminal alkynes, CO2, and various allylic, propargylic or benzylic chlorides to exclusively yield function