Cu-Catalyzed [1,3]-Fluorine Rearrangement Reactions of <i>N</i> -Fluoroanilines

carbon in a site-selective manner. DFT calculations suggested that the reaction proceeds via the coordination of a Cu(III) species to fluoride and aniline nitrogen, followed by C-F bond formation through a nucleophilic attack by the fluoride.

Authors

Institutions

Publication Details

Journal
Organic Letters
Published
2026-04-01
DOI
https://doi.org/10.1021/acs.orglett.6c01176
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00

Funders

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

Cu-Catalyzed [1,3]-Fluorine Rearrangement Reactions of N -Fluoroanilines

Itaru Nakamura, Takuma Sato, Mao Suzuki, Masahiro Terada
Organic Letters
Fluorine in Organic Chemistry
article

Cu-Catalyzed [1,3]-Fluorine Rearrangement Reactions of N -Fluoroanilines

Itaru Nakamura, Takuma Sato, Mao Suzuki, Masahiro Terada
article en

Abstract

carbon in a site-selective manner. DFT calculations suggested that the reaction proceeds via the coordination of a Cu(III) species to fluoride and aniline nitrogen, followed by C-F bond formation through a nucleophilic attack by the fluoride.

Organic LettersVol. 28(14)
Tohoku University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 31%
Fluorine in Organic Chemistry
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.

Cu-Catalyzed [1,3]-Fluorine Rearrangement Reactions of <i>N</i> -Fluoroanilines — Itaru Nakamura, Takuma Sato, et al. · Organic Letters (2026) | TGRS Research Map | TGRS