Department of Biological and Synthetic Chemistry, Center of Biomedical Research, SGPGIMS Campus, Raebareli Road, Lucknow 226014, Uttar Pradesh, India.
Sci Adv. 2023 Apr 21;9(16):eadg3311. doi: 10.1126/sciadv.adg3311.
Transition metal-catalyzed C─H bond activation and borylation is a powerful synthetic method that offers versatile synthetic transformation from organoboron compounds to virtually all other functional groups. Compared to the ortho-borylation, remote borylation remains more challenging owing to the inaccessibility of these C─H bonds. Enforcing the metal catalyst toward the remote C─H bonds needs well-judged catalyst design through proper ligand development. This review article aims to summarize the recent discoveries for the remote C─H borylation by the employment of new catalyst/ligand design with the help of steric of the ligand, noncovalent interactions. It has been found that C─H borylation now takes part in the total synthesis of natural products in a shorter route. Whereas, Ir-catalyzed C─H borylation is predominant, cobalt catalyst has also started to affect this field for sustainable and cost-effective development.
过渡金属催化的 C─H 键活化和硼化是一种强大的合成方法,它提供了从有机硼化合物到几乎所有其他官能团的多功能合成转化。与邻位硼化相比,由于这些 C─H 键不易接近,远程硼化仍然更具挑战性。通过适当的配体开发来对金属催化剂进行远程 C─H 键的强制作用需要进行精心判断的催化剂设计。本文综述了通过配体的空间位阻、非共价相互作用等手段,利用新型催化剂/配体设计对远程 C─H 硼化反应的最新发现。现已发现,C─H 硼化现在可以通过更短的路线参与到天然产物的全合成中。而 Ir 催化的 C─H 硼化占主导地位,钴催化剂也已开始影响这一领域,以实现可持续和具有成本效益的发展。