Electrochemical Regioselective C-3 Alkoxycarbonylation of 2<i>H</i>-Indazoles

This study describes an efficient electrochemical synthetic method for C-3 alkoxycarbonylation of 2<i>H</i>-indazoles with carbazates under constant current in an undivided cell without the need for external oxidants or metal catalysts. This methodology exhibits broad functional group compatibility, affording the products with good yields. Easy scalability and drug diversification demonstrate the synthetic efficacy and applicability of this protocol.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-05-23
DOI
https://doi.org/10.1021/acs.joc.5c00785
Citations
4
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
3.74

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article

Electrochemical Regioselective C-3 Alkoxycarbonylation of 2H-Indazoles

Duddu S. Sharada, Jagadeesh Reddy Thondur, Gedu Satyanarayana, Punith S Gowda
4 citations
The Journal of Organic Chemistry
Radical Photochemical Reactions
3.74
article

Electrochemical Regioselective C-3 Alkoxycarbonylation of 2H-Indazoles

Duddu S. Sharada, Jagadeesh Reddy Thondur, Gedu Satyanarayana, Punith S Gowda
article en
4 citations

Abstract

This study describes an efficient electrochemical synthetic method for C-3 alkoxycarbonylation of 2<i>H</i>-indazoles with carbazates under constant current in an undivided cell without the need for external oxidants or metal catalysts. This methodology exhibits broad functional group compatibility, affording the products with good yields. Easy scalability and drug diversification demonstrate the synthetic efficacy and applicability of this protocol.

The Journal of Organic ChemistryVol. 90(22)
Pondicherry University (IN), Indian Institute of Technology Hyderabad (IN)
Council of Scientific and Industrial Research, India, Ministry of Education, India, Science and Engineering Research Board
Clean water and sanitation
Openalex Percentile: Top 7%
Radical Photochemical Reactions
3.74
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