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Copper catalysed amidation of aryl halides through chelation assistance
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. (BMC ; BBCL)ORCID iD: 0000-0003-0774-2528
Kings Coll London, UK.
Kings Coll London, UK.
Linnaeus University, Faculty of Health and Life Sciences, Department of Chemistry and Biomedical Sciences. Uppsala University. (BMC ; BBCL)ORCID iD: 0000-0002-0407-6542
2015 (English)In: Chemical Communications, ISSN 1359-7345, E-ISSN 1364-548X, Vol. 51, no 23, p. 4834-4837Article in journal (Refereed) Published
Abstract [en]

A copper mediated C-N bond formation for the amidation of aryl halides using 8-aminoquinoline has been developed. This strategy provides efficient access to amides bearing two contiguous heterocyclic moieties and does not require the presence of additional ligands.

Place, publisher, year, edition, pages
2015. Vol. 51, no 23, p. 4834-4837
National Category
Chemical Sciences
Research subject
Chemistry, Organic Chemistry
Identifiers
URN: urn:nbn:se:lnu:diva-42145DOI: 10.1039/c4cc09940kISI: 000351056200021PubMedID: 25695680Scopus ID: 2-s2.0-84924351944OAI: oai:DiVA.org:lnu-42145DiVA, id: diva2:801913
Available from: 2015-04-10 Created: 2015-04-10 Last updated: 2018-05-17Bibliographically approved

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Kathiravan, SuppanNicholls, Ian A.

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