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Mechanochemical synthesis of aromatic ketones: pyrylium tetrafluoroborate mediated deaminative arylation of amides
Department of Chemistry, Faculty of Natural Sciences, Matej Bel University, Tajovského 40 97401 Banska Bystrica, Slovakia.
Department of Heteroatom Chemistry, Institute of Organic Chemistry, National Academy of Sciences of Ukraine, 5 Murmans'ka Kyiv 02660, Ukraine.
Department of Biology/Chemistry, Center for Cellular Nanoanalytics (CellNanOs), Universität Osnabrück, Barbarastr. 7 D-49076 Osnabrück, Germany.
Department of Chemistry, Faculty of Natural Sciences, Matej Bel University, Tajovského 40 97401 Banska Bystrica, Slovakia.
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2024 (English)In: Chemical Science, ISSN 2041-6520, E-ISSN 2041-6539, Vol. 15, no 24, p. 9155-9163Article in journal (Refereed) Published
Abstract [en]

A new method has been introduced that is able to tackle the complexities of N-C(O) activation in amide moieties through utilization of pyrylium tetrafluoroborate in a mechanochemical setting, where amide bonds undergo activation and subsequent conversion to biaryl ketones. Due to the employment of a mechanochemical setting, the reaction conforms to green chemistry principles, offering an environmentally friendly approach to traditional amide derivatization techniques that rely on transition metals to achieve further functionalization.

Place, publisher, year, edition, pages
Royal Society of Chemistry (RSC) , 2024. Vol. 15, no 24, p. 9155-9163
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Organic Chemistry
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URN: urn:nbn:se:kth:diva-366887DOI: 10.1039/d4sc00904eISI: 001226961000001PubMedID: 38903233Scopus ID: 2-s2.0-85193818585OAI: oai:DiVA.org:kth-366887DiVA, id: diva2:1983487
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QC 20250711

Available from: 2025-07-11 Created: 2025-07-11 Last updated: 2025-07-11Bibliographically approved

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Iaroshenko, Viktor O.

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