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Electrochemical rhodium catalysed alkyne annulation with pyrazoles through anodic oxidation - a metal oxidant/additive free methodology
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. Attana AB, Sweden.ORCID iD: 0000-0003-0774-2528
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. (Linnaeus Ctr Biomat Chem, BMC;BBCL)ORCID iD: 0000-0003-1981-4533
2023 (English)In: Organic and biomolecular chemistry, ISSN 1477-0520, E-ISSN 1477-0539, Vol. 21, no 9, p. 2024-2033Article in journal (Refereed) Published
Abstract [en]

Pyrazole and its derivatives are important azole heteroarenes prevalent in pharmaceutical compounds and have been used as ligands for protein binding, making them valuable targets for synthetic applications. Herein we disclose an electrochemical intermolecular C-H/N-H oxidative annulation of 2-phenylpyrazoles with alkynes using a rhodium(iii) redox regime without any external metal oxidants in a water compatible solvent system. Both symmetrical and unsymmetrical alkynes were shown to be compatible with the optimized conditions.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2023. Vol. 21, no 9, p. 2024-2033
National Category
Organic Chemistry
Research subject
Chemistry, Organic Chemistry
Identifiers
URN: urn:nbn:se:lnu:diva-119823DOI: 10.1039/d2ob02306gISI: 000937287700001PubMedID: 36790440Scopus ID: 2-s2.0-85148745118OAI: oai:DiVA.org:lnu-119823DiVA, id: diva2:1744322
Available from: 2023-03-17 Created: 2023-03-17 Last updated: 2023-05-31Bibliographically approved

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Kathiravan, SuppanAnaspure, Prasad

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