A Green Synthetic Approach to Construct C2‐Quaternary Indolin‐3‐Ones at Room Temperature via Regioselective Oxidative Dearomatization of Indoles

Abstract A new synthetic strategy for the construction of C2‐quaternary indole for the formation of Indolin‐3‐ones has been explored via indium(III) trifluoromethansulphonate catalyst at room temperature with TBHP as a green oxidant in water. This approach for the oxidative dearomatization process allows for the production of the natural product Halichrome A and a broad range of C2‐arylated Indolin‐3‐ones under a milder condition in very good yields. The oxidative self‐dimerization and self‐trimerization of various indole derivatives have also been achieved under the same conditions.

Authors

Institutions

Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-12-07
DOI
https://doi.org/10.1002/ejoc.202401037
Citations
3
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.75
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A Green Synthetic Approach to Construct C2‐Quaternary Indolin‐3‐Ones at Room Temperature via Regioselective Oxidative Dearomatization of Indoles

Parasuraman Jaisankar, Muhammad Rafi, Sudip Dey, Pinaki Bhattacharjee et al.
3 citations
European Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
0.75
article

A Green Synthetic Approach to Construct C2‐Quaternary Indolin‐3‐Ones at Room Temperature via Regioselective Oxidative Dearomatization of Indoles

Parasuraman Jaisankar, Muhammad Rafi, Sudip Dey, Pinaki Bhattacharjee, Sandeep Kar, S. Rajendra Prasad
article en
3 citations

Abstract

Abstract A new synthetic strategy for the construction of C2‐quaternary indole for the formation of Indolin‐3‐ones has been explored via indium(III) trifluoromethansulphonate catalyst at room temperature with TBHP as a green oxidant in water. This approach for the oxidative dearomatization process allows for the production of the natural product Halichrome A and a broad range of C2‐arylated Indolin‐3‐ones under a milder condition in very good yields. The oxidative self‐dimerization and self‐trimerization of various indole derivatives have also been achieved under the same conditions.

European Journal of Organic ChemistryVol. 28(2)
Commonwealth Scientific and Industrial Research Organisation (AU), Indian Institute of Chemical Biology (IN), Academy of Scientific and Innovative Research (IN)
Openalex Percentile: Top 31%
Catalytic C–H Functionalization Methods
0.75
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.

A Green Synthetic Approach to Construct C2‐Quaternary Indolin‐3‐Ones at Room Temperature via Regioselective Oxidative Dearomatization of Indoles — Parasuraman Jaisankar, Muhammad Rafi, et al. · European Journal of Organic Chemistry (2024) | TGRS Research Map | TGRS