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Recent advances in electrochemical C–N bond formation via C–H/N–H activation with hydrogen evolution
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. Attana AB, Sweden. (Linnaeus Ctr Biomat Chem, BMC;BBCL)ORCID iD: 0000-0003-0774-2528
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. Linnaeus University, Linnaeus Knowledge Environments, Advanced Materials. (Linnaeus Ctr Biomat Chem, BMC;BBCL)ORCID iD: 0000-0002-0407-6542
2024 (English)In: Current Research in Green and Sustainable Chemistry, E-ISSN 2666-0865, Vol. 8, article id 100405Article in journal (Refereed) Published
Abstract [en]

Electroorganic synthesis is a powerful sustainable tool for achieving greener and more efficient chemical processes across various industries. By adhering to the principles of green chemistry, atom economy, and resource efficiency, electroorganic synthesis can play a pivotal role in addressing environmental concerns and promoting a more sustainable future for chemical production. This review focuses on the latest advancements in the emerging application of electrochemistry in C-N bond formation through C-H/N-H cross-coupling. The first part of the review describes the electrochemical amination of arenes using metal catalysis (Cu, Co, Ni) with directing groups on the arene moiety. The next section addresses the same type of electrochemical C-N bond formation on arenes without directing groups, which represents a more general strategy enabling the synthesis of anilines and various heterocyclic-bound arenes in high yields. Further developments on benzylic systems are also discussed. This is followed by developments in the combination of photocatalysis and electrochemistry to activate C-H bonds in arenes, alkanes, and benzylic systems, including the use of flow reactor configurations for these reactions.

Place, publisher, year, edition, pages
Elsevier, 2024. Vol. 8, article id 100405
National Category
Organic Chemistry
Research subject
Chemistry, Organic Chemistry
Identifiers
URN: urn:nbn:se:lnu:diva-128661DOI: 10.1016/j.crgsc.2024.100405Scopus ID: 2-s2.0-85187989064OAI: oai:DiVA.org:lnu-128661DiVA, id: diva2:1849672
Funder
Swedish Research Council, 2023–03406Swedish Research Council, 2014–4573Linnaeus UniversityHelge Ax:son Johnsons stiftelse , 2022–0317The Crafoord FoundationAvailable from: 2024-04-08 Created: 2024-04-08 Last updated: 2025-03-20Bibliographically approved

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Kathiravan, SuppanNicholls, Ian A.

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