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作 者:Wen Peng Mai Jin Wei Yuan Zhi Cheng Li Gang Chun Sun
机构地区:[1]Chemistry and Chemical Engineering School,Henan University of Technology,Zhengzhou 450001,China
出 处:《Chinese Chemical Letters》2012年第2期185-188,共4页中国化学快报(英文版)
基 金:Henan University of Technology for financial support(The Introduction of Talent Fund)
摘 要:An efficient palladium-catalyzed copper- and amine-free Sonogashira coupling reaction of aryl bromides and chlorides was studied using a sterically hindered monooxychlorophosphine as new ligand.The use of 2 mol%Pd(OAc)_2 in the presence of K_2CO_3 allows the coupling reaction to proceed at mild condition with good to excellent yields.An efficient palladium-catalyzed copper- and amine-free Sonogashira coupling reaction of aryl bromides and chlorides was studied using a sterically hindered monooxychlorophosphine as new ligand.The use of 2 mol%Pd(OAc)_2 in the presence of K_2CO_3 allows the coupling reaction to proceed at mild condition with good to excellent yields.
关 键 词:Palladium Copper-free Coupling Sonogashira reaction Chlorophosphine
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