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超越 Friedel 和 Crafts:芳环中 C-H 键的固有烷基化。

Beyond Friedel and Crafts: Innate Alkylation of C-H Bonds in Arenes.

机构信息

Laboratoire de Chimie Organique, Service de Chimie et Physico-Chimie Organiques, Université libre de Bruxelles (ULB), Avenue F.D. Roosevelt 50, CP160/06, 1050, Brussels, Belgium.

出版信息

Angew Chem Int Ed Engl. 2019 Jun 3;58(23):7558-7598. doi: 10.1002/anie.201806631. Epub 2019 Apr 4.

Abstract

Alkylated arenes are ubiquitous molecules and building blocks commonly utilized in most areas of science. Despite its apparent simplicity, the regioselective alkylation of arenes is still a challenging transformation in a lot of cases. Classical methods for the introduction of alkyl groups to arenes, such as the venerable Friedel-Crafts reaction, radical additions, metalation or prefunctionalization of the arene followed by further alkylation, as well as alternatives such as the directed alkylation of C-H bonds, still suffer from severe limitations in terms of scope, efficiency, and selectivity. This can be addressed by exploiting the innate reactivity of some (hetero)arenes, in which electronic and steric properties, governed (or not) by the presence of one (or multiple) heteroatom(s), ensure high levels of regioselectivity. These innate alkylations of C-H bonds in (hetero)arenes will be overviewed comprehensively in this Review.

摘要

烷基芳烃是普遍存在的分子和结构单元,广泛应用于科学的大多数领域。尽管其结构看似简单,但芳烃的区域选择性烷基化在很多情况下仍然是一个具有挑战性的转化过程。将烷基基团引入芳烃的经典方法,如古老的傅-克反应、自由基加成、芳烃的金属化或预官能化,然后进一步烷基化,以及其他方法,如 C-H 键的定向烷基化,在范围、效率和选择性方面仍然存在严重的限制。通过利用某些(杂)芳烃的固有反应性可以解决这些问题,其中电子和空间性质(或不受)一个(或多个)杂原子的存在,可确保高区域选择性。本综述将全面概述(杂)芳烃中 C-H 键的固有烷基化反应。

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