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首页> 外文期刊>Organometallics >Dehydrogenative synthesis of imines from alcohols and amines catalyzed by a ruthenium N-heterocyclic carbene complex
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Dehydrogenative synthesis of imines from alcohols and amines catalyzed by a ruthenium N-heterocyclic carbene complex

机译:N-杂环卡宾络合物催化的醇和胺的亚胺脱氢合成

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摘要

A new method for the direct synthesis of imines from alcohols and amines is described where hydrogen gas is liberated. The reaction is catalyzed by the ruthenium N-heterocyclic carbene complex [RuCl _2(IiPr)(p-cymene)] in the presence of the ligand DABCO and molecular sieves. The imination can be applied to a variety of primary alcohols and amines and can be combined with a subsequent addition reaction. A deuterium labeling experiment indicates that the catalytically active species is a ruthenium dihydride. The reaction is believed to proceed by initial dehydrogenation of the alcohol to the aldehyde, which stays coordinated to ruthenium. Nucleophilic attack of the amine affords the hemiaminal, which is released from ruthenium and converted into the imine.
机译:描述了一种从醇和胺直接合成亚胺的新方法,其中释放出氢气。在配体DABCO和分子筛的存在下,钌N-杂环卡宾络合物[RuCl _2(IiPr)(p-cymene)]催化该反应。酰亚胺化可应用于多种伯醇和胺,并可与随后的加成反应结合。氘标记实验表明,催化活性物质是二氢化钌。据信该反应是通过将醇最初脱氢为醛而进行的,醛与钌保持配位。胺的亲核攻击提供了半胱氨酸,其从钌释放并转化为亚胺。

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