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首页> 外文期刊>Science Advances >n-Alkanes to n-alcohols: Formal primary C─H bond hydroxymethylation via quadruple relay catalysis
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n-Alkanes to n-alcohols: Formal primary C─H bond hydroxymethylation via quadruple relay catalysis

机译:N-烷烃至N-醇:正规初级C─H键羟甲基甲基化通过四重继电器催化

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摘要

Nature is able to synergistically combine multiple enzymes to conduct well-ordered biosynthetic transformations. Mimicking nature’s multicatalysis in vitro may give rise to new chemical transformations via interplay of numerous molecular catalysts in one pot. The direct and selective conversion of abundant n -alkanes to valuable n -alcohols is a reaction with enormous potential applicability but has remained an unreached goal. Here, we show that a quadruple relay catalysis system involving three discrete transition metal catalysts enables selective synthesis of n -alcohols via n -alkane primary C─H bond hydroxymethylation. This one-pot multicatalysis system is composed of Ir-catalyzed alkane dehydrogenation, Rh-catalyzed olefin isomerization and hydroformylation, and Ru-catalyzed aldehyde hydrogenation. This system is further applied to synthesis of α,ω-diols from simple α-olefins through terminal-selective hydroxymethylation of silyl alkanes.
机译:性质能够协同结合多种酶来进行有序的生物合成转化。在体外模仿性质的多分析可以通过在一个罐中的许多分子催化剂的相互作用产生新的化学转化。丰富的N-alkanes对宝贵的N - 醇的直接和选择性转化为具有巨大潜在适用性的反应,但仍然是未联系的目标。在这里,我们表明,涉及三个离散过渡金属催化剂的四重继电器催化系统能够通过N-alkane初级C─H键羟甲基化选择性合成N-醇。该一锅多分析系统由IR催化的烷烃脱氢,RH催化的烯烃异构化和加氢甲酰化,以及Ru催化的醛氢化。该系统进一步应用于通过甲硅烷基烷烃的末端选择性羟甲基化学来合成来自简单α-烯烃的α,ω-二醇。

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