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作 者:Wen Yan Hao Jian Wen Jiang Ming Zhong Cai
机构地区:[1]Department of Chemistry, Jiangxi Normal University, Nanchang 330022, China
出 处:《Chinese Chemical Letters》2007年第7期773-776,共4页中国化学快报(英文版)
基 金:the National Natural Science Foundation of China(No.20462002);Natural Science Foundation of Jiangxi Province(No.0420015)for financial support.
摘 要:(E)-α-Iodovinyl sulfones 1 underwent the Sonogashira coupling reactions with terminal alkynes 2 in piperidine at room temperature in the presence of 5 mol% of Pd(PPh3)4 and 10 mol% of CuI to stereospecifically afford the corresponding (Z)-2-sulfonyl-substituted 1,3-enynes 3 in high yields.(E)-α-Iodovinyl sulfones 1 underwent the Sonogashira coupling reactions with terminal alkynes 2 in piperidine at room temperature in the presence of 5 mol% of Pd(PPh3)4 and 10 mol% of CuI to stereospecifically afford the corresponding (Z)-2-sulfonyl-substituted 1,3-enynes 3 in high yields.
关 键 词:(E)-α-Iodovinyl sulfone 1 3-Enynylsulfone Sonogashira coupling Terminal alkyne
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