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.
CITATION STYLE
Hassan, M. M. M., Guria, S., Dey, S., Das, J., & Chattopadhyay, B. (2023, April 21). Transition metal–catalyzed remote C-H borylation: An emerging synthetic tool. Science Advances. American Association for the Advancement of Science. https://doi.org/10.1126/sciadv.adg3311
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