Preparation of pseudocyclic I( <scp>iii</scp> ) reagents and their application in selective oxidations

Four <i>N</i>,<i>N</i>-disubstituted pseudocyclic-type iodine(III) reagents were conveniently prepared in excellent yields from <i>ortho</i>-iodobenzamides using <i>m</i>CPBA as the oxidant under mild conditions. This class of hypervalent iodine(III) oxidants exhibited remarkable selectivity in oxidizing sulfides solely to sulfoxides, without any detectable sulfone formation, even when used in excess or at elevated temperatures. Mechanistically, the nucleophilic attack of sulfide generates the sulfonium intermediate, which enables the oxidation of sulfides.

Authors

Institutions

Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-12-04
DOI
https://doi.org/10.1039/d5ob01641j
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

Preparation of pseudocyclic I( iii ) reagents and their application in selective oxidations

Shuoshuo Zhang, Dan Xiao, Yunfei Du, Cong Li et al.
Organic & Biomolecular Chemistry
Oxidative Organic Chemistry Reactions
article

Preparation of pseudocyclic I( iii ) reagents and their application in selective oxidations

Shuoshuo Zhang, Dan Xiao, Yunfei Du, Cong Li, Yong You, Xiangyu Zhan
article en

Abstract

Four <i>N</i>,<i>N</i>-disubstituted pseudocyclic-type iodine(III) reagents were conveniently prepared in excellent yields from <i>ortho</i>-iodobenzamides using <i>m</i>CPBA as the oxidant under mild conditions. This class of hypervalent iodine(III) oxidants exhibited remarkable selectivity in oxidizing sulfides solely to sulfoxides, without any detectable sulfone formation, even when used in excess or at elevated temperatures. Mechanistically, the nucleophilic attack of sulfide generates the sulfonium intermediate, which enables the oxidation of sulfides.

Organic & Biomolecular ChemistryVol. 24(2)
Tianjin University (CN), Tianjin Economic-Technological Development Area (CN)
Openalex Percentile: Top 71%
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.