Tang Xinxin, Jia Xiangqing, Huang Zheng
State Key Laboratory of Organometallic Chemistry , Shanghai Institute of Organic Chemistry , University of Chinese Academy of Sciences , Chinese Academy of Sciences , 345 Lingling Road , Shanghai 200032 , China . Email:
Chem Sci. 2017 Nov 9;9(2):288-299. doi: 10.1039/c7sc03610h. eCollection 2018 Jan 14.
The conversion of vast low-value saturated hydrocarbons into valuable chemicals is of great interest. Thanks to the progression of organometallic and coordination chemistry, transition metal catalysed C sp-H bond functionalisation has now become a powerful tool for alkane transformations. Specifically, methods for alkane functionalisation include radical initiated C-H functionalisation, carbene/nitrene insertion, and transition metal catalysed C-H bond activation. This perspective provides a systematic and concise overview of each protocol, highlighting the factors that govern regioselectivity in these reactions. The challenges of the existing catalytic tactics and future directions for catalyst development in this field will be presented.
将大量低价值的饱和烃转化为有价值的化学品备受关注。得益于有机金属化学和配位化学的发展,过渡金属催化的C sp-H键官能化现已成为烷烃转化的有力工具。具体而言,烷烃官能化方法包括自由基引发的C-H官能化、卡宾/氮宾插入以及过渡金属催化的C-H键活化。本文综述了每种方法,强调了这些反应中区域选择性的影响因素,并讨论了现有催化策略面临的挑战以及该领域催化剂开发的未来方向。