Aryldiazonium tetrafluoroborate salts as green and efficient coupling partners for the Suzuki-Miyaura reaction : from optimisation to mole scale
Colleville, Aymeric P. and Horan, Richard A. J. and Tomkinson, Nick C. O. (2014) Aryldiazonium tetrafluoroborate salts as green and efficient coupling partners for the Suzuki-Miyaura reaction : from optimisation to mole scale. Organic Process Research and Development, 18 (9). 1128–1136. ISSN 1083-6160 (https://doi.org/10.1021/op5002353)
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Abstract
The use of aryldiazonium tetrafluoroborate salts as coupling partners in the Suzuki-Miyaura reaction was investigated from a process chemistry perspective including safety evaluation, solvent and catalyst screening and multi-variate factor optimization. Optimised conditions were applied to a range of substrates to evaluate the scope and limitations of the reaction and one example was carried out on mole-scale to demonstrate the practicality and scalability of the process
ORCID iDs
Colleville, Aymeric P. ORCID: https://orcid.org/0000-0003-3094-5155, Horan, Richard A. J. and Tomkinson, Nick C. O. ORCID: https://orcid.org/0000-0002-5509-0133;-
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Item type: Article ID code: 56512 Dates: DateEvent12 August 2014Published12 August 2014AcceptedSubjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry Depositing user: Pure Administrator Date deposited: 25 May 2016 11:01 Last modified: 11 Nov 2024 10:49 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/56512