Naphthylpyridyl–Cu(II)-Catalyzed Oxidative Coupling of 2-Naphthylamines to Access BINAM Derivatives
In this study, we report the efficient synthesis of 1,1'-binaphthyl-2,2'-diamine (BINAM) derivatives via copper-catalyzed oxidative coupling of 2-aminonaphthalenes. The use of a ligand featuring an extended π system in combination with Cu(II) and molecular oxygen as the terminal oxidant enabled the formation of various BINAM derivatives in yields of up to 84%. Mechanistic investigations suggest a redox pathway involving Cu(II)/Cu(I) cycling, and π-π interactions between the ligand and substrate are proposed to stabilize reactive intermediates, thereby contributing to the observed efficiency.
Authors
- Daeyeon Lee
- Houng Kang (ORCID: https://orcid.org/0000-0001-5587-5689)
- Jong‐Hyeon Lee (ORCID: https://orcid.org/0000-0003-3193-9128)
- Min Kim (ORCID: https://orcid.org/0000-0002-1710-2682)
- Jooyeon Lee (ORCID: https://orcid.org/0000-0001-5220-0950)
- M. S. KONG
- Jiwon Kang (ORCID: https://orcid.org/0009-0006-0270-402X)
Institutions
- Chungbuk National University (KR)
- Seowon University (KR)
- Anyang University (KR)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-08-08
- DOI
- https://doi.org/10.1021/acs.orglett.5c02740
- Citations
- 1
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.94
Funders
- National Research Foundation of Korea