17603-76-8Relevant articles and documents
Copper-catalyzed silylation reactions of propargyl epoxides: Easy access to 2,3-allenols and stereodefined alkenes
Chang, Xi-Hao,Liu, Zheng-Li,Luo, Yun-Cheng,Yang, Chao,Liu, Xiao-Wei,Da, Bing-Chao,Li, Jie-Jun,Ahmad, Tanveer,Loh, Teck-Peng,Xu, Yun-He
supporting information, p. 9344 - 9347 (2017/08/23)
Efficient silylation reactions of propargyl epoxides catalyzed by copper catalysts have been developed. Under mild reaction conditions, tri- and tetra-substituted functionalized allenols and alkenes could be selectively obtained in moderate to high yields
Beyond the limits: Palladium-N-heterocyclic carbene-based catalytic system enables highly efficient [4+2] benzannulation reactions
Zatolochnaya, Olga V.,Galenko, Alexey V.,Gevorgyan, Vladimir
supporting information; experimental part, p. 1149 - 1155 (2012/06/16)
A highly efficient catalytic system for the palladium-catalyzed [4+2] benzannulation reaction of enynes and enynophiles has been developed. The use of an N-heterocyclic carbene-based palladium precursor allowed us to achieve turnover numbers up to 1800. T