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作 者:Shuai Zhang Xinhua Duan Pengfei Li
机构地区:[1]Frontier Institute of Science and Technology,Xi'an Jiaotong University,Xi'an,Shaanxi 710054,China [2]School of Chemistry,Xi'an Jiaotong University,Xi'an,Shaanxi 710049,China [3]State Key Laboratory of Elemento-Organic Chemistry,Nankai University,Tianjin 300071,China [4]Xi'an Key Laboratory of Sustainable Energy Materials Chemistry,Xi'an Jiaotong University,Xi'an,Shaanxi 710049,China
出 处:《Chinese Journal of Chemistry》2021年第3期590-596,共7页中国化学(英文版)
基 金:the National Natural Sci-ence Foundation of China(Nos.21672168,21971202);the Key Laboratory Construction Program of Xi'an Municipal Bureau of Science and Technology(No.201805056ZD7CG40)。
摘 要:Main observation and conclusion Stereodefinedβ,γ-unsaturated carbony|compounds are important yet synthetically challenging units in natural products and drugs.Disclosed herein is a mild,rapid copper-catalyzed diborylation reaction of cross-conjugated enynones as a step-economic and modular approach to stereodefined multifunctionalizedβ,γ-unsaturated ketones by fine control of chemo-,regio-,Z/E and diastereoselectivity.The substrate scope was examined and a possible catalytic cycle was proposed to explain the multifaceted selectivity.
关 键 词:STEREOSELECTIVITY β γ-Unsaturated ketones Copper catalysis BORYLATION Cross-conjugated enynones
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