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.

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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

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article

Oxidative Coupling of Alcohols and Amines Using Functionalized Cu(II) 2-Quinoxolinol Salen Catalysts

John D. Gorden, A. E. V. Gorden, Ansh Chugh, Xiaoyu Huo et al.
ACS Omega
Asymmetric Hydrogenation and Catalysis
article

Oxidative Coupling of Alcohols and Amines Using Functionalized Cu(II) 2-Quinoxolinol Salen Catalysts

John D. Gorden, A. E. V. Gorden, Ansh Chugh, Xiaoyu Huo, Raymond Hicks
article en

Abstract

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.

ACS OmegaVol. 11(6)
Texas Tech University (US)
Texas Tech University
Openalex Percentile: Top 69%
Asymmetric Hydrogenation and Catalysis
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