Oxidative Coupling of Alcohols and Amines Using Functionalized Cu(II) 2-Quinoxolinol Salen Catalysts
Cu-(II) complexes bearing 2-quinoxolinol salen ligands have been prepared and studied for direct imine formation by oxidative coupling between alcohols and amines, with <i>tert</i>-butyl hydroperoxide (TBHP) as an oxidant under mild conditions. Various aromatic alcohols are coupled to anilines and benzylamines to form the corresponding imines in good-to-excellent yields. Notably, the water formed was the principal byproduct in 2 steps. This is a greener and more powerful approach as alcohols are readily accessible materials, enabling the synthesis of a diverse range of imine products.
Authors
- John D. Gorden (ORCID: https://orcid.org/0000-0002-0304-1954)
- A. E. V. Gorden
- Ansh Chugh
- Xiaoyu Huo
- Raymond Hicks
Institutions
- Texas Tech University (US)
Publication Details
- Journal
- ACS Omega
- Published
- 2026-02-03
- DOI
- https://doi.org/10.1021/acsomega.5c10891
- Primary Topic
- Asymmetric Hydrogenation and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Texas Tech University