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铁催化硝基芳烃参与的烯烃的厌氧 Mukaiyama 型水合反应。

Fe-Catalyzed Anaerobic Mukaiyama-Type Hydration of Alkenes using Nitroarenes.

机构信息

Organisch-Chemisches Institut, Westfalische Wilhelms-Universität, Corrensstraße 40, 48149, Münster, Germany.

出版信息

Angew Chem Int Ed Engl. 2021 Apr 6;60(15):8313-8320. doi: 10.1002/anie.202015740. Epub 2021 Mar 3.

Abstract

Hydration of alkenes using first row transition metals (Fe, Co, Mn) under oxygen atmosphere (Mukaiyama-type hydration) is highly practical for alkene functionalization in complex synthesis. Different hydration protocols have been developed, however, control of the stereoselectivity remains a challenge. Herein, highly diastereoselective Fe-catalyzed anaerobic Markovnikov-selective hydration of alkenes using nitroarenes as oxygenation reagents is reported. The nitro moiety is not well explored in radical chemistry and nitroarenes are known to suppress free radical processes. Our findings show the potential of cheap nitroarenes as oxygen donors in radical transformations. Secondary and tertiary alcohols were prepared with excellent Markovnikov-selectivity. The method features large functional group tolerance and is also applicable for late-stage chemical functionalization. The anaerobic protocol outperforms existing hydration methodology in terms of reaction efficiency and selectivity.

摘要

使用第一过渡金属(铁、钴、锰)在氧气氛围下对烯烃进行水合反应(Mukaiyama 型水合)在复杂合成中对烯烃的官能化具有很高的实用性。已经开发了不同的水合方法,但是立体选择性的控制仍然是一个挑战。本文报道了使用硝基芳烃作为氧源,通过铁催化实现烯烃的高非对映选择性厌氧 Markovnikov 选择性水合。硝基部分在自由基化学中尚未得到充分探索,并且已知硝基芳烃会抑制自由基过程。我们的研究结果表明,廉价的硝基芳烃在自由基转化中作为氧供体具有潜力。通过该方法可以以优异的 Markovnikov 选择性制备仲醇和叔醇。该方法具有广泛的官能团容忍性,也适用于后期的化学官能化。在反应效率和选择性方面,该厌氧方案优于现有的水合方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70f0/8049001/1330f82836dc/ANIE-60-8313-g002.jpg

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