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通过氢 borrowing 或氢自转移的 3d-金属催化的 N-和 C-烷基化反应。

3d-Metal Catalyzed N- and C-Alkylation Reactions via Borrowing Hydrogen or Hydrogen Autotransfer.

机构信息

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

出版信息

Chem Rev. 2019 Feb 27;119(4):2524-2549. doi: 10.1021/acs.chemrev.8b00306. Epub 2018 Nov 20.

Abstract

The conservation of our element resources is a fundamental challenge of mankind. The development of alcohol refunctionalization reactions is a possible fossil carbon conservation strategy since alcohols can be obtained from indigestible and abundantly available biomass. The conservation of our rare noble metals, frequently used in key technologies such as catalysis, might be feasible by replacing them with highly abundant metals. The alkylation of amines by alcohols and related C-C coupling reactions are early examples of alcohol refunctionalization reactions. These reactions follow mostly the borrowing hydrogen or hydrogen autotransfer catalysis concept, and many 3d-metal catalysts have been disclosed in recent years. In this review, we summarize the progress made in developing Cu, Ni, Co, Fe, and Mn catalysts for C-N and C-C bond formation reactions with alcohols and amines using the borrowing hydrogen or hydrogen autotransfer concept. We expect that the findings in this field will inspire others to develop new efficient and selective earth-abundant metal catalysts for borrowing hydrogen or hydrogen autotransfer applications or to develop novel alcohol refunctionalization reactions that can be mediated by such metals.

摘要

保护我们的元素资源是人类面临的一项基本挑战。醇的重新功能化反应的发展是一种可能的节约化石碳的策略,因为醇可以从难以消化和丰富的生物质中获得。通过用丰富的金属替代稀有贵金属(这些贵金属经常用于催化等关键技术),可能可以节约我们的稀有贵金属。醇与胺的烷基化和相关的 C-C 偶联反应是醇的重新功能化反应的早期例子。这些反应主要遵循借氢或氢自动转移催化的概念,近年来已经披露了许多 3d 金属催化剂。在这篇综述中,我们总结了使用借氢或氢自动转移概念开发用于 C-N 和 C-C 键形成反应的 Cu、Ni、Co、Fe 和 Mn 催化剂的进展。我们希望这一领域的发现将激励其他人开发用于借氢或氢自动转移应用的新的高效和选择性的丰富地球金属催化剂,或开发可以由这些金属介导的新型醇的重新功能化反应。

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