Halogenation-enabled intramolecular deaminative cyclization
Carbon-nitrogen (C-N) bonds are traditionally inert toward nucleophilic attack. Herein, we present a halogenation-induced C-N bond activation strategy that enables the intramolecular substitution of secondary and tertiary amino groups by hydroxyl, amino, carboxyl, or thiol groups, providing an efficient method for amine transformation.
Authors
- Gang He (ORCID: https://orcid.org/0000-0002-9064-3418)
- Wenbo Wang
Institutions
- Nankai University (CN)
Publication Details
- Journal
- Organic & Biomolecular Chemistry
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5ob00535c
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Fundamental Research Funds for the Central Universities