SNAr-Functionalization of Diaryliodonium Salts: Access to Densely Substituted Arenes

Abstract Diaryliodonium salts are efficient electrophilic arylation reagents for a wide variety of nucleophiles. The main limitation in the arylation scope is often the difficulty in synthesizing advanced heteroatom-functionalized diaryliodonium salts, due to their sensitivity to acidic and oxidative conditions. We present a general SNAr strategy to functionalize fluoro-substituted iodonium salts, which enables the synthesis of a wide range of heteroatom-functionalized iodonium salts, with demonstrated reactivity in a variety of transition-metal-free O-, N-, and S-arylations to provide densely functionalized aromatic products.

Authors

Institutions

Publication Details

Journal
JACS Au
Published
2026-09-10
DOI
https://doi.org/10.1021/jacsau.6c01053
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

SNAr-Functionalization of Diaryliodonium Salts: Access to Densely Substituted Arenes

Berit Olofsson, Leonard Kersting, Erika Linde, Judith Braunreuther
JACS Au
Oxidative Organic Chemistry Reactions
article

SNAr-Functionalization of Diaryliodonium Salts: Access to Densely Substituted Arenes

Berit Olofsson, Leonard Kersting, Erika Linde, Judith Braunreuther
article en

Abstract

Abstract Diaryliodonium salts are efficient electrophilic arylation reagents for a wide variety of nucleophiles. The main limitation in the arylation scope is often the difficulty in synthesizing advanced heteroatom-functionalized diaryliodonium salts, due to their sensitivity to acidic and oxidative conditions. We present a general SNAr strategy to functionalize fluoro-substituted iodonium salts, which enables the synthesis of a wide range of heteroatom-functionalized iodonium salts, with demonstrated reactivity in a variety of transition-metal-free O-, N-, and S-arylations to provide densely functionalized aromatic products.

JACS Au
Stockholm University (SE)
Clean water and sanitation
Openalex Percentile: Top 20%
Oxidative Organic Chemistry Reactions
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.