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钌催化羰基化合物的选择性硼氢化反应。

Ruthenium Catalyzed Selective Hydroboration of Carbonyl Compounds.

机构信息

School of Chemical Sciences, National Institute of Science Education and Research (NISER) , Bhubaneswar-751 005, India.

出版信息

Org Lett. 2015 Oct 2;17(19):4790-3. doi: 10.1021/acs.orglett.5b02352.

Abstract

Using the [Ru(p-cymene)Cl2]2 (1) complex, catalytic hydroboration of aldehydes and ketones with pinacolborane under neat and mild conditions is reported. At rt, chemoselective hydroboration of aldehydes over the ketones is also attained. Mechanistic studies confirmed the immediate formation of monohydride bridged dinuclear complex [{(η(6)-p-cymene)RuCl}2(μ-H-μ-Cl)] (1b) from the reaction of 1 with pinacolborane, which catalyzed the highly efficient hydroboration reactions. The catalytic cycle containing mononuclear Ru-H species and intramolecular 1,3-hydride transfer is postulated.

摘要

本文报道了使用[Ru(p-cymene)Cl2]2(1)复合物,在温和条件下,使频哪醇硼烷对醛酮进行催化氢化硼烷化反应。在室温下,该反应还可选择性地对醛进行氢化硼烷化。机理研究证实,1 与频哪醇硼烷反应立即生成桥连单氢的双核配合物 [{(η(6)-p-cymene)RuCl}2(μ-H-μ-Cl)](1b),该配合物可催化高效的氢化硼烷化反应。该催化循环包含单核 Ru-H 物种和分子内 1,3-氢转移。

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