Hartwig John F, Larsen Matthew A
Department of Chemistry, University of California, Berkeley, California 94720, United States; Division of Chemical Sciences, Lawrence Berkeley Laboratory, Berkeley, California 94720, United States.
ACS Cent Sci. 2016 May 25;2(5):281-92. doi: 10.1021/acscentsci.6b00032. Epub 2016 May 2.
The functionalization of C-H bonds has created new approaches to preparing organic molecules by enabling new strategic "disconnections" during the planning of a synthetic route. Such functionalizations also have created the ability to derivatize complex molecules by modifying one or more of the many C-H bonds. For these reasons, researchers are developing new types of functionalization reactions of C-H bonds and new applications of these processes. These C-H bond functionalization reactions can be divided into two general classes: those directed by coordination to an existing functional group prior to the cleavage of the C-H bond (directed) and those occurring without coordination prior to cleavage of the C-H bond (undirected). The undirected functionalizations of C-H bonds are much less common and more challenging to develop than the directed reactions. This outlook will focus on undirected C-H bond functionalization, as well as related reactions that occur by a noncovalent association of the catalyst prior to C-H bond cleavage. The inherent challenges of conducting undirected functionalizations of C-H bonds and the methods for undirected functionalization that are being developed will be presented, along with the factors that govern selectivity in these reactions. Finally, this outlook discusses future directions for research on undirected C-H functionalization, with an emphasis on the limitations that must be overcome if this type of methodology is to become widely used in academia and in industry.
C-H键的官能团化通过在合成路线设计过程中实现新的策略性“切断”,为有机分子的制备创造了新方法。这种官能团化还使得通过修饰众多C-H键中的一个或多个来衍生化复杂分子成为可能。基于这些原因,研究人员正在开发新型的C-H键官能团化反应以及这些反应的新应用。这些C-H键官能团化反应可大致分为两类:一类是在C-H键断裂之前通过与现有官能团配位来引导反应(导向反应),另一类是在C-H键断裂之前不发生配位的反应(非导向反应)。与导向反应相比,C-H键的非导向官能团化不太常见且开发起来更具挑战性。本综述将聚焦于非导向C-H键官能团化以及在C-H键断裂之前通过催化剂的非共价缔合发生的相关反应。将介绍进行C-H键非导向官能团化所固有的挑战以及正在开发的非导向官能团化方法,以及这些反应中决定选择性的因素。最后,本综述讨论了非导向C-H官能团化的未来研究方向,重点强调了若要使这类方法在学术界和工业界得到广泛应用必须克服的局限性。