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机构地区:[1]Department of Chemistry, Tongji University, Shanghai 200092, China [2]Shenyang Research Institute of Chemical Industry Co., Ltd., Shenyang, Liaoning 110021, China
出 处:《Chinese Journal of Chemistry》2011年第11期2350-2354,共5页中国化学(英文版)
基 金:Project supported by the National Natural Science Foundation of China (No. 30873153) and the Key Projects of Shanghai in Biomedical (No. 08431902700).
摘 要:A convenient, efficient, and generally applicable method was developed for the synthesis of terminal alkynes from anti-3-aryl-2,3-dibromopropanoic acids in the presence of DMSO and K2CO3.A convenient, efficient, and generally applicable method was developed for the synthesis of terminal alkynes from anti-3-aryl-2,3-dibromopropanoic acids in the presence of DMSO and K2CO3.
关 键 词:elimination alkynes anti-3-aryl-2 3-dibromopropanoic acids K2CO3
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