Iron-Catalysed Chemo-, Regio-, and Stereoselective Hydrosilylation of Alkenes and Alkynes using a Bench-Stable Iron(II) Pre-Catalyst

被引:159
作者
Greenhalgh, Mark D. [1 ]
Frank, Dominik J. [1 ]
Thomas, Stephen P. [1 ]
机构
[1] Univ Edinburgh, Sch Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
基金
英国工程与自然科学研究理事会;
关键词
catalysis; hydrosilylation; iron; olefins; synthetic methods; ORGANIC-SYNTHESIS; SILAFUNCTIONAL COMPOUNDS; DEACTIVATION PATHWAYS; CARBON BOND; COMPLEXES; HYDROGENATION; REDUCTION; HALIDES; HYDROBORATION; OXIDATION;
D O I
10.1002/adsc.201300827
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The chemo-, regio-, and stereoselective iron-catalysed hydrosilylation of alkenes and alkynes with excellent functional group tolerance is reported (34 examples, 41-96% yield). The catalyst and reagents are commercially available and easy to handle, with the active iron catalyst being generated in situ, thus providing a simple and practical methodology for iron-catalysed hydrosilylation. The silane products can be oxidised to the anti-Markovnikov product of olefin hydration, and the one-pot iron-catalysed hydrosilylation-oxidation of olefins to give silane(di)ols directly is also reported. The iron pre-catalyst was used at loadings as low as 0.07mol%, and displayed catalyst turnover frequencies (TOF) approaching 60,000molh(-1). Initial mechanistic studies indicate an iron(I) active catalyst.
引用
收藏
页码:584 / 590
页数:7
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