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

Institutions

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

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Naphthylpyridyl–Cu(II)-Catalyzed Oxidative Coupling of 2-Naphthylamines to Access BINAM Derivatives

Daeyeon Lee, Houng Kang, Jong‐Hyeon Lee, Min Kim et al.
1 citations
Organic Letters
Catalytic C–H Functionalization Methods
0.94
article

Naphthylpyridyl–Cu(II)-Catalyzed Oxidative Coupling of 2-Naphthylamines to Access BINAM Derivatives

Daeyeon Lee, Houng Kang, Jong‐Hyeon Lee, Min Kim, Jooyeon Lee, M. S. KONG, Jiwon Kang
article en
1 citations

Abstract

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.

Organic LettersVol. 27(33)
Chungbuk National University (KR), Seowon University (KR), Anyang University (KR)
National Research Foundation of Korea
Clean water and sanitation
Openalex Percentile: Top 23%
Catalytic C–H Functionalization Methods
0.94
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Naphthylpyridyl–Cu(II)-Catalyzed Oxidative Coupling of 2-Naphthylamines to Access BINAM Derivatives — Daeyeon Lee, Houng Kang, et al. · Organic Letters (2025) | TGRS Research Map | TGRS