Iron‐Catalyzed Reductive Alkylation of Imines via Ligand‐to‐Metal Charge Transfer
Abstract Herein, we report a sustainable, iron‐catalyzed reductive alkylation reaction of imines with carboxylic acids and unactivated hydrocarbons to access synthetically relevant amine motifs. The reaction proceeds via a light‐induced ligand‐to‐metal charge transfer (LMCT) process, generating alkyl radicals either through a decarboxylative pathway or by forming a reactive chlorine radical that facilitates hydrogen atom transfer (HAT) with alkanes. This photochemical transformation offers several advantages, including sustainability, mild reaction conditions, cost efficiency, and an excellent atom economy.
Authors
- Serik Zhumagazy (ORCID: https://orcid.org/0000-0001-7214-6146)
- Kuntal Pal (ORCID: https://orcid.org/0000-0002-9005-0874)
- Magnus Rueping (ORCID: https://orcid.org/0000-0003-4580-5227)
Institutions
- King Abdullah University of Science and Technology (SA)
Publication Details
- Journal
- ChemCatChem
- Published
- 2025-09-24
- DOI
- https://doi.org/10.1002/cctc.202501210
- Citations
- 3
- Primary Topic
- Asymmetric Hydrogenation and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 1.61