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锰催化醇和氨基醇合成吡咯

Manganese-Catalyzed Sustainable Synthesis of Pyrroles from Alcohols and Amino Alcohols.

机构信息

Inorganic Chemistry II-Catalyst Design, University of Bayreuth, 95440, Bayreuth, Germany.

Organometallic Chemistry, Adam Mickiewicz University, 61614, Poznań, Poland.

出版信息

Angew Chem Int Ed Engl. 2017 Jun 12;56(25):7261-7265. doi: 10.1002/anie.201702543. Epub 2017 May 16.

Abstract

The development of reactions that convert alcohols into important chemical compounds saves our fossil carbon resources as alcohols can be obtained from indigestible biomass such as lignocellulose. The conservation of our rare noble metals is of similar importance, and their replacement by abundantly available transition metals, such as Mn, Fe, or Co (base or nonprecious metals), in key technologies such as catalysis is a promising option. Herein, we report on the first base-metal-catalyzed synthesis of pyrroles from alcohols and amino alcohols. The most efficient catalysts are Mn complexes stabilized by PN P ligands whereas related Fe and Co complexes are inactive. The reaction proceeds under mild conditions at catalyst loadings as low as 0.5 mol %, and has a broad scope and attractive functional-group tolerance. These findings may inspire others to use Mn catalysts to replace Ir or Ru complexes in challenging dehydrogenation reactions.

摘要

醇类可以从难以消化的生物质如木质纤维素中获得,将醇类转化为重要化合物的反应的发展可以节省我们的化石碳资源。同样重要的是保护我们稀有的贵金属,在催化等关键技术中用丰富的过渡金属(如 Mn、Fe 或 Co(基础或非贵金属)替代它们是一个很有前景的选择。在此,我们报告了首例基于碱金属的醇类和氨基醇类合成吡咯的方法。最有效的催化剂是由 PN P 配体稳定的 Mn 配合物,而相关的 Fe 和 Co 配合物则没有活性。该反应在催化剂负载低至 0.5 mol%的温和条件下进行,具有广泛的适用范围和良好的官能团耐受性。这些发现可能会激励其他人使用 Mn 催化剂来替代 Ir 或 Ru 配合物,以进行具有挑战性的脱氢反应。

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