Cs<sub>2</sub>CO<sub>3</sub>-Mediated Annulation of Cyclopropane-1,1-dicarbonitriles with <i>o</i>-Benzenediamines: Access to Substituted 2-Aminoquinoxalines

The Cs<sub>2</sub>CO<sub>3</sub>-mediated formal (4 + 2) cascade annulation strategy for the synthesis of 2-aminoquinoxalines has been developed using D-A cyclopropanes and <i>o</i>-benzenediamines as the substrates. The protocol provides an efficient method of accessing a broad range of 2-aminoquinoxaline derivatives in good to excellent yields with good functional-group tolerance.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-03-28
DOI
https://doi.org/10.1021/acs.joc.4c03160
Citations
1
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
0.94

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article

Cs2CO3-Mediated Annulation of Cyclopropane-1,1-dicarbonitriles with o-Benzenediamines: Access to Substituted 2-Aminoquinoxalines

Cunde Wang, Haiwen Li, Xinyi Wan, Wenzhe Cheng
1 citations
The Journal of Organic Chemistry
Cyclopropane Reaction Mechanisms
0.94
article

Cs2CO3-Mediated Annulation of Cyclopropane-1,1-dicarbonitriles with o-Benzenediamines: Access to Substituted 2-Aminoquinoxalines

Cunde Wang, Haiwen Li, Xinyi Wan, Wenzhe Cheng
article en
1 citations

Abstract

The Cs<sub>2</sub>CO<sub>3</sub>-mediated formal (4 + 2) cascade annulation strategy for the synthesis of 2-aminoquinoxalines has been developed using D-A cyclopropanes and <i>o</i>-benzenediamines as the substrates. The protocol provides an efficient method of accessing a broad range of 2-aminoquinoxaline derivatives in good to excellent yields with good functional-group tolerance.

The Journal of Organic ChemistryVol. 90(14)
Yangzhou University (CN)
Priority Academic Program Development of Jiangsu Higher Education Institutions
Openalex Percentile: Top 28%
Cyclopropane Reaction Mechanisms
0.94
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