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DOI: 10.1055/a-1890-8375
Transition-Metal-Catalyzed Regioselective C–H Borylation of Pyridines
We are grateful for the financial support provided by the National Natural Science Foundation of China (21871204).


Abstract
The C–H borylation strategy has spurred intense research endeavors due to the high atom- and step-economy it represents and because of the broad range of utilities of the resulting organoboranes. Nevertheless, this powerful transformation has had limited substrate scope and poor regioselectivity when it was applied to Lewis basic substrates (e.g., azines). The basic functionalities in substrates can coordinate to the metal centers, hindering the formation of products. Herein, we provide a brief overview of recent advances in transition-metal-catalyzed regioselective C–H borylation of pyridines. Attention is paid to the latest contributions, which have demonstrated remarkable regioselectivity.
1 Introduction
2 para-Selective C−H Borylation
3 meta-Selective C−H Borylation
4 ortho-Selective C−H Borylation
5 Summary
Publikationsverlauf
Eingereicht: 15. Juni 2022
Angenommen nach Revision: 03. Juli 2022
Accepted Manuscript online:
03. Juli 2022
Artikel online veröffentlicht:
29. Juli 2022
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