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铁催化的简单和复杂叔胺的α-C-H 氰化反应。

Iron-Catalyzed α-C-H Cyanation of Simple and Complex Tertiary Amines.

机构信息

Department of Chemistry and Biochemistry, Worcester Polytechnic Institute, 100 Institute Road, Worcester, Massachusetts 01609, United States.

Department of Chemistry, Faculty of Arts and Sciences, Mersin University, 33343 Mersin, Turkey.

出版信息

J Org Chem. 2021 Feb 5;86(3):2489-2498. doi: 10.1021/acs.joc.0c02642. Epub 2021 Jan 19.

Abstract

This manuscript details the development of a general and mild protocol for the α-C-H cyanation of tertiary amines and its application in late-stage functionalization. Suitable substrates include tertiary aliphatic, benzylic, and aniline-type substrates and complex substrates. Functional groups tolerated under the reaction conditions include various heterocycles and ketones, amides, olefins, and alkynes. This broad substrate scope is remarkable, as comparable reaction protocols for α-C-H cyanation frequently occur via free radical mechanisms and are thus fundamentally limited in their functional group tolerance. In contrast, the presented catalyst system tolerates functional groups that typically react with free radicals, suggesting an alternative reaction pathway. All components of the described catalyst system are readily available, allowing implementation of the presented methodology without the need for lengthy catalyst synthesis.

摘要

本文详细介绍了一种通用且温和的叔胺α-C-H 氰化反应方案的开发及其在后期官能团化中的应用。适用的底物包括叔脂肪族、苄基和苯胺型底物以及复杂底物。在反应条件下耐受的官能团包括各种杂环和酮、酰胺、烯烃和炔烃。这种广泛的底物范围是显著的,因为可比的α-C-H 氰化反应方案通常通过自由基机制发生,因此在官能团耐受性方面受到根本限制。相比之下,所提出的催化剂体系耐受通常与自由基反应的官能团,表明存在替代的反应途径。所描述的催化剂体系的所有组分都易于获得,允许在不需要冗长的催化剂合成的情况下实施所提出的方法。

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