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Pd(OAc)_2催化的α-溴代二硫缩烯酮与芳基硼酸的Suzuki-Miyaura偶联反应 被引量:1

Pd(OAc)_2-catalyzed Suzuki-Miyaura coupling reaction of α-bromo ketene dithioacetals with arylboronic acids
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摘要 C-C键的形成反应是有机化学中最重要的基本反应.本文发展了一种简单、有效钯催化的α-溴代二硫缩烯酮与芳基硼酸的Suzuki-Miyaura偶联反应.该反应的实现,不仅建立了一种简单、有效合成α-芳基-α-烯酰基二硫缩烯酮化合物新方法,而且扩展了α-溴代二硫缩烯酮类化合物在有机合成中的进一步应用. C-C bond formation is one of the most important reactions in organic synthesis.Here,a simple and efficient Pd(OAc)2-catalyzed Suzuki-Miyaura coupling reaction of α-bromo ketene dithioacetals with arylboronic acids has been developed.The reaction not only provides a simple,efficient,and new method for the synthesis of α-aryl-α-cinnamoyl ketene dithioacetals,but also further expands the synthetic potential of α-bromo ketene dithioacetals in organic synthesis.
出处 《分子科学学报》 CAS CSCD 北大核心 2016年第4期298-301,共4页 Journal of Molecular Science
基金 国家自然科学基金基金资助项目(21172032)
关键词 α-溴代二硫缩烯酮 芳基硼酸 Suzuki-Miyaura偶联 钯催化剂 α-bromo ketene dithioacetal arylboronic acid Suzuki–Miyaura coupling palladium catalyst
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