Advances in NN Bond Formation: Mechanistic Diversity and Emerging Catalytic Strategies

The nitrogen–nitrogen (NN) bond is ubiquitous in organic compounds, yet efficient synthetic strategies for the direct construction of NN bonds remain challenging. Well‐known approaches, such as oxidative dehydrogenative coupling (ODC) and reductive coupling (RC), have provided valuable routes for forming NN linkages. Nitrene transfer strategies emerged as a complementary and increasingly versatile platform. The distinct electronic structures of classical closed‐shell nitrenoids (Fischer‐ and Schrock‐type), open‐shell nitrene radical intermediates, and photochemically generated nitrene species primarily govern NN bond‐forming selectivity. The use of electrochemical, photochemical, and biocatalytic approaches continues to expand the scope of sustainable synthetic chemistry. This review summarizes recent advances in ODC, RC, nitrene transfer chemistry, photochemical, electrochemical, and enzymatic approaches for NN bond formation, with particular emphasis on reaction design, mechanistic insights, and synthetic applications.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-09-29
DOI
https://doi.org/10.1002/ejoc.70839
Primary Topic
Radical Photochemical Reactions
Type
article
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article

Advances in NN Bond Formation: Mechanistic Diversity and Emerging Catalytic Strategies

Subhajit Chakraborty, Afsana Pervin, Nanda Dulal Paul
European Journal of Organic Chemistry
Radical Photochemical Reactions
article

Advances in NN Bond Formation: Mechanistic Diversity and Emerging Catalytic Strategies

Subhajit Chakraborty, Afsana Pervin, Nanda Dulal Paul
article en

Abstract

The nitrogen–nitrogen (NN) bond is ubiquitous in organic compounds, yet efficient synthetic strategies for the direct construction of NN bonds remain challenging. Well‐known approaches, such as oxidative dehydrogenative coupling (ODC) and reductive coupling (RC), have provided valuable routes for forming NN linkages. Nitrene transfer strategies emerged as a complementary and increasingly versatile platform. The distinct electronic structures of classical closed‐shell nitrenoids (Fischer‐ and Schrock‐type), open‐shell nitrene radical intermediates, and photochemically generated nitrene species primarily govern NN bond‐forming selectivity. The use of electrochemical, photochemical, and biocatalytic approaches continues to expand the scope of sustainable synthetic chemistry. This review summarizes recent advances in ODC, RC, nitrene transfer chemistry, photochemical, electrochemical, and enzymatic approaches for NN bond formation, with particular emphasis on reaction design, mechanistic insights, and synthetic applications.

European Journal of Organic Chemistry
Indian Institute of Engineering Science and Technology, Shibpur (IN)
Openalex Percentile: Top 23%
Radical Photochemical Reactions
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Advances in NN Bond Formation: Mechanistic Diversity and Emerging Catalytic Strategies — Subhajit Chakraborty, Afsana Pervin, et al. · European Journal of Organic Chemistry (2026) | TGRS Research Map | TGRS