Electrochemical Selenized Reaction of <i>N</i>-Arylbicyclo[1.1.0]butane-1-carboxamides: Access to 3-(Arylselanyl)spiro[cyclobutane-1,3′-indolin]-2′-one Derivatives

A novel selenized reaction of <i>N</i>-arylbicyclo [1.1.0]butane-1-carboxamides with diselenide for the synthesis of polycyclic indoline derivatives is developed under electrochemical conditions. The synthesis is achieved by the bicyclo[1.1.0]butane strain-release reaction and intramolecular cyclization process. In addition, this approach features a wide range of substrates, good group tolerance, shorter reaction time, and mild conditions.

Authors

Institutions

Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-10-23
DOI
https://doi.org/10.1021/acs.joc.4c02085
Citations
16
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
4.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Electrochemical Selenized Reaction of N-Arylbicyclo[1.1.0]butane-1-carboxamides: Access to 3-(Arylselanyl)spiro[cyclobutane-1,3′-indolin]-2′-one Derivatives

Liangce Rong, Yuliang Qian, Haicheng Zhao, Qin Zheng-long et al.
16 citations
The Journal of Organic Chemistry
Radical Photochemical Reactions
4.00
article

Electrochemical Selenized Reaction of N-Arylbicyclo[1.1.0]butane-1-carboxamides: Access to 3-(Arylselanyl)spiro[cyclobutane-1,3′-indolin]-2′-one Derivatives

Liangce Rong, Yuliang Qian, Haicheng Zhao, Qin Zheng-long, Yun Liu, Zifeng Zhang, Jiyao Liu
article en
16 citations

Abstract

A novel selenized reaction of <i>N</i>-arylbicyclo [1.1.0]butane-1-carboxamides with diselenide for the synthesis of polycyclic indoline derivatives is developed under electrochemical conditions. The synthesis is achieved by the bicyclo[1.1.0]butane strain-release reaction and intramolecular cyclization process. In addition, this approach features a wide range of substrates, good group tolerance, shorter reaction time, and mild conditions.

The Journal of Organic ChemistryVol. 89(21)
Jiangsu Normal University (CN)
Openalex Percentile: Top 5%
Radical Photochemical Reactions
4.00
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.