Palladium-catalyzed synthesis of aryl amides through silanoate-mediated hydrolysis of nitriles
McPherson, Christopher G. and Livingstone, Keith and Jamieson, Craig and Simpson, Iain (2016) Palladium-catalyzed synthesis of aryl amides through silanoate-mediated hydrolysis of nitriles. Synlett, 27 (1). pp. 88-92. ISSN 0936-5214 (https://doi.org/10.1055/s-0035-1560724)
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Abstract
A procedure for the formation of aryl amides through the palladium-catalyzed coupling of nitriles and aryl bromides, via the formation of intermediary silanoate derived imidate species is reported. Optimization was undertaken and examples of the process are described that furnish the products in up to 86% isolated yield.
ORCID iDs
McPherson, Christopher G. ORCID: https://orcid.org/0000-0002-3082-0515, Livingstone, Keith, Jamieson, Craig ORCID: https://orcid.org/0000-0002-6567-8272 and Simpson, Iain;-
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Item type: Article ID code: 55929 Dates: DateEvent4 January 2016Published9 October 2015Published Online25 September 2015AcceptedNotes: Dedicated to Professor Steven V. Ley on the occasion of his 70th birthday Subjects: Science > Chemistry > Physical and theoretical chemistry Department: Faculty of Science > Pure and Applied Chemistry Depositing user: Pure Administrator Date deposited: 17 Mar 2016 15:38 Last modified: 11 Nov 2024 11:17 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/55929
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