铜催化芳基环丙烷开环硅氢化和硼氢化反应

IF 5.7 1区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chinese Journal of Chemistry Pub Date : 2024-11-11 DOI:10.1002/cjoc.202400811
Zhen-Yu Xiao, Zi-Lu Wang, Yun-He Xu
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引用次数: 0

摘要

芳基环丙烷(ACPs)是高度应变的底物,可以很容易地用于各种转化。本研究展示了铜催化acp开环硅氢化和硼氢化反应的结果,展示了C-C键的精确切割。该反应提供了一种简便有效的制备硅烷和硼酸盐的方法。
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Copper-Catalyzed Ring-Opening Hydrosilylation and Hydroboration of Arylidenecyclopropanes

Arylidenecyclopropanes (ACPs) are highly strained substrates that can be readily utilized for diverse transformations. This study showcases the outcomes of copper-catalyzed ring-opening hydrosilylation and hydroboration reactions of ACPs, showcasing precise cleavage of C—C bonds. The reaction presents an effective and convenient method for producing homoallylic silanes and boronates.

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来源期刊
Chinese Journal of Chemistry
Chinese Journal of Chemistry 化学-化学综合
CiteScore
8.80
自引率
14.80%
发文量
422
审稿时长
1.7 months
期刊介绍: The Chinese Journal of Chemistry is an international forum for peer-reviewed original research results in all fields of chemistry. Founded in 1983 under the name Acta Chimica Sinica English Edition and renamed in 1990 as Chinese Journal of Chemistry, the journal publishes a stimulating mixture of Accounts, Full Papers, Notes and Communications in English.
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