Biomimetic Iron-Catalyzed Oxidation of 3-Substituted Indoles to 2-Oxindoles

A biomimetic iron-catalyzed system has been developed for the selective oxidation of 3-substituted indoles to 3-monosubstituted 2-oxindoles using H<sub>2</sub>O<sub>2</sub> as a green oxidant under mild conditions. This catalytic approach addresses the drawbacks of stoichiometric biomimetic models and exhibits broad substrate scope and excellent functional group tolerance. Mechanistic studies suggest the reaction proceeds via an epoxide intermediate followed by a 2,3-hydride shift, with the epoxidation step being rate-determining. The method provides a sustainable route to biologically relevant 2-oxindole scaffolds.

Authors

Institutions

Publication Details

Journal
Organic Letters
Published
2026-02-09
DOI
https://doi.org/10.1021/acs.orglett.6c00165
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Biomimetic Iron-Catalyzed Oxidation of 3-Substituted Indoles to 2-Oxindoles

Changyin Zhao, Lei Liu, Hongbin Liu, Jiazheng Wu et al.
Organic Letters
Catalytic C–H Functionalization Methods
article

Biomimetic Iron-Catalyzed Oxidation of 3-Substituted Indoles to 2-Oxindoles

Changyin Zhao, Lei Liu, Hongbin Liu, Jiazheng Wu, Minghui Zhu, Lei Liu
article en

Abstract

A biomimetic iron-catalyzed system has been developed for the selective oxidation of 3-substituted indoles to 3-monosubstituted 2-oxindoles using H<sub>2</sub>O<sub>2</sub> as a green oxidant under mild conditions. This catalytic approach addresses the drawbacks of stoichiometric biomimetic models and exhibits broad substrate scope and excellent functional group tolerance. Mechanistic studies suggest the reaction proceeds via an epoxide intermediate followed by a 2,3-hydride shift, with the epoxidation step being rate-determining. The method provides a sustainable route to biologically relevant 2-oxindole scaffolds.

Organic LettersVol. 28(7)
Shandong University (CN), City University of Hong Kong, Shenzhen Research Institute (CN), Shandong First Medical University (CN)
Responsible consumption and production
Openalex Percentile: Top 61%
Catalytic C–H Functionalization Methods
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.