Front Cover: Light Driven Acid and Base Controlled Selective Synthesis of 3,4‐Dihydroquinoxalinones and Quinoxalinones via Cascade Cyclization of Aryl Diazoacetates With <i>o</i> ‐Phenylenediamines (Eur. J. Org. Chem. 14/2026)

The Front Cover shows the acid–base-controlled selective synthesis of 3,4-dihydroquinoxalinones and quinoxalinones through photoredox cascade cyclization of aryl diazoacetates with o-phenylenediamines. The red and blue colors symbolize the reaction pathway environments under acidic and basic conditions, respectively, and the ambient molecular oxygen represents an environmentally benign oxidant for the synthesis of quinoxalinone derivatives. More information can be found in the Research Article by R. Anandhan and co-workers (DOI: 10.1002/ejoc.202500963).

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-04-15
DOI
https://doi.org/10.1002/ejoc.70456
Primary Topic
Synthesis and Biological Evaluation
Type
article
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article

Front Cover: Light Driven Acid and Base Controlled Selective Synthesis of 3,4‐Dihydroquinoxalinones and Quinoxalinones via Cascade Cyclization of Aryl Diazoacetates With o ‐Phenylenediamines (Eur. J. Org. Chem. 14/2026)

Kesavan Prasanth, Ramasamy Anandhan, Pakkirisamy Nithishkumar
European Journal of Organic Chemistry
Synthesis and Biological Evaluation
article

Front Cover: Light Driven Acid and Base Controlled Selective Synthesis of 3,4‐Dihydroquinoxalinones and Quinoxalinones via Cascade Cyclization of Aryl Diazoacetates With o ‐Phenylenediamines (Eur. J. Org. Chem. 14/2026)

Kesavan Prasanth, Ramasamy Anandhan, Pakkirisamy Nithishkumar
article en

Abstract

The Front Cover shows the acid–base-controlled selective synthesis of 3,4-dihydroquinoxalinones and quinoxalinones through photoredox cascade cyclization of aryl diazoacetates with o-phenylenediamines. The red and blue colors symbolize the reaction pathway environments under acidic and basic conditions, respectively, and the ambient molecular oxygen represents an environmentally benign oxidant for the synthesis of quinoxalinone derivatives. More information can be found in the Research Article by R. Anandhan and co-workers (DOI: 10.1002/ejoc.202500963).

European Journal of Organic ChemistryVol. 29(14)
University of Madras (IN)
Life in Land
Openalex Percentile: Top 10%
Synthesis and Biological Evaluation
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