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铱催化的通过导向和空间位阻效应促进的内部炔烃的区域选择性硅氢化反应。

Iridium-catalyzed regioselective hydrosilylation of internal alkynes facilitated by directing and steric effects.

机构信息

State Key Laboratory of Organic-Inorganic Composites, College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, China.

出版信息

Org Biomol Chem. 2021 Jul 21;19(28):6216-6220. doi: 10.1039/d1ob00910a.

Abstract

Here we reported the iridium-catalyzed hydrosilylation of internal alkynes under simple and mild conditions. The intrinsic functional groups of alkyne substrates were disclosed to be crucial in facilitating both the hydrosilylation process and related regioselectivity owing to their coordination capability towards the iridium catalyst. Utilization of the steric trimethylsilyl-protected trihydroxysilane proved to be another critical factor in ensuring the efficient proceeding of this process.

摘要

在这里,我们报道了铱催化的在简单温和条件下的内炔烃的硅氢化反应。炔烃底物的内在官能团被证明在促进硅氢化反应过程和相关区域选择性方面是至关重要的,因为它们对铱催化剂具有配位能力。利用空间位阻的三甲基硅基保护的三羟基硅烷被证明是确保这个过程高效进行的另一个关键因素。

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