A divergent electrochemical platform for diazene radical generation and C–N coupling reactions
Open Access
- 4 March 2026
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Organic Chemistry Frontiers
- Vol. 13 (9) , 2749-2761
Abstract
The development of sustainable methods for controlled C–N bond formation remains a central challenge in modern synthesis.Keywords
Funding Information
- Anusandhan National Research Foundation (CRG/2023/001272)
This publication has 33 references indexed in Scilit:
- Visible-light-promoted multi-component carbene transfer reactions of diazo compounds via ring-opening of cyclic ethersChinese Chemical Letters, 2025
- Towards Sustainable Materials: A Review of Acylhydrazone Chemistry for Reversible PolymersChemistry – A European Journal, 2024
- Nitrogen-Centered Radicals in Functionalization of sp2 Systems: Generation, Reactivity, and Applications in SynthesisChemical Reviews, 2022
- When Light Meets Nitrogen-Centered Radicals: From Reagents to CatalystsAccounts of Chemical Research, 2020
- Alkyl Carbazates for Electrochemical Deoxygenative Functionalization of HeteroarenesAngewandte Chemie International Edition, 2020
- N‐Centered Radical Directed Remote C−H Bond Functionalization via Hydrogen Atom TransferChemistry – An Asian Journal, 2020
- Hydroxylamine Derivatives as Nitrogen‐Radical Precursors in Visible‐Light PhotochemistryChemistry – A European Journal, 2018
- Microwave-assisted synthesis, characterization and bioassay of acylhydrazone derivatives as influenza neuraminidase inhibitorsMedicinal Chemistry Research, 2017
- Iron‐Catalyzed Oxidative Addition of Alkoxycarbonyl Radicals to Alkenes with Carbazates and AirAngewandte Chemie International Edition, 2010
- Synthesis and biological activities of diflunisal hydrazide–hydrazonesEuropean Journal of Medicinal Chemistry, 2003