Transition-metal-free electrophilic amination of boronic acid derivatives
Abstract Extensive efforts have been devoted to the development of new methodologies for C−N bond-forming reactions to access valuable nitrogen-containing organic molecules. Growing interest in transition-metal (TM)-free processes, which serve as indispensable tools for greener and more efficient synthesis, has led to the development of TM-free electrophilic amination of readily available organoboron compounds as a promising approach. This highlight review summarizes recent advances in the TM-free electrophilic amination of boronic acid derivatives, which have greatly expanded the scope and efficiency of amine synthesis.
Authors
- Satoshi Minakata (ORCID: https://orcid.org/0000-0001-9619-445X)
- Kensuke Kiyokawa (ORCID: https://orcid.org/0000-0001-6124-2861)
Institutions
- The University of Osaka (JP)
Publication Details
- Journal
- Chemistry Letters
- Published
- 2025-11-28
- DOI
- https://doi.org/10.1093/chemle/upaf215
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Japan Society for the Promotion of Science
- Japan Science and Technology Agency
- Precursory Research for Embryonic Science and Technology