Electrochemical Oxidative Dibrominative Cyclization of 1,n-Enynes with Hypervalent Iodoarene Intermediates Utilizing Recyclable Bromine Ionic Liquids

An electrochemical approach with iodoarene as a mediator using recyclable ionic liquids to achieve dibromonative cyclization of 1,n-enynes has been reported. With recyclable bromine sources, <i>in situ</i> generation of iodine(III) compounds through electrochemical oxidation to achieve cyclization, a variety of heterocyclic frameworks containing both vinyl and alkyl bromide groups had been obtained in high yields with good selectivity.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-04-05
DOI
https://doi.org/10.1021/acs.joc.5c00049
Citations
2
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
1.87

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article

Electrochemical Oxidative Dibrominative Cyclization of 1,n-Enynes with Hypervalent Iodoarene Intermediates Utilizing Recyclable Bromine Ionic Liquids

Longji Li, Yang’en You, Xu Wang, Huaibin Jiang
2 citations
The Journal of Organic Chemistry
Oxidative Organic Chemistry Reactions
1.87
article

Electrochemical Oxidative Dibrominative Cyclization of 1,n-Enynes with Hypervalent Iodoarene Intermediates Utilizing Recyclable Bromine Ionic Liquids

Longji Li, Yang’en You, Xu Wang, Huaibin Jiang
article en
2 citations

Abstract

An electrochemical approach with iodoarene as a mediator using recyclable ionic liquids to achieve dibromonative cyclization of 1,n-enynes has been reported. With recyclable bromine sources, <i>in situ</i> generation of iodine(III) compounds through electrochemical oxidation to achieve cyclization, a variety of heterocyclic frameworks containing both vinyl and alkyl bromide groups had been obtained in high yields with good selectivity.

The Journal of Organic ChemistryVol. 90(15)
Hefei University of Technology (CN), First Affiliated Hospital of Zhengzhou University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Henan Province, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 17%
Oxidative Organic Chemistry Reactions
1.87
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