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过渡金属催化的使用格氏试剂促进的氯硅烷进行的碳-硅键形成反应。

Transition metal catalyzed carbon-silicon bond forming reactions using chlorosilanes promoted by Grignard reagents.

作者信息

Terao Jun, Kambe Nobuaki

机构信息

Department of Applied Chemistry & Center for Atomic and Molecular Technologies Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

Chem Rec. 2007;7(1):57-67. doi: 10.1002/tcr.20101.

Abstract

New catalytic C--Si bond-forming reactions using chlorosilanes are described. These reactions proceed efficiently under mild conditions by the combined use of Grignard reagents and transition metal catalysts, such as Ti, Zr, Ni, and Pd. It is proposed that ate complex intermediates formed by the reaction of transition metals with Grignard reagents play important roles as the active catalytic species. The present study demonstrates the practical use of chlorosilanes in transition metal catalyzed silylation reactions providing convenient methods for allyl- or vinylsilane synthesis. The reaction pathways of these transformations as well as the scope and limitations are discussed.

摘要

描述了使用氯硅烷的新型催化碳-硅键形成反应。通过联合使用格氏试剂和过渡金属催化剂(如钛、锆、镍和钯),这些反应在温和条件下能高效进行。有人提出,过渡金属与格氏试剂反应形成的酸根络合物中间体作为活性催化物种发挥着重要作用。本研究证明了氯硅烷在过渡金属催化的硅烷化反应中的实际应用,为烯丙基硅烷或乙烯基硅烷的合成提供了便捷方法。讨论了这些转化反应的途径以及范围和局限性。

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