Base-free nickel-catalysed decarbonylative Suzuki–Miyaura coupling of acid fluorides
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Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41586-018-0628-7.pdf
Reference33 articles.
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2. Brown, D. G. & Boström, J. Analysis of past and present synthetic methodologies on medicinal chemistry: where have all the new reactions gone? J. Med. Chem. 59, 4443–4458 (2016).
3. Lennox, A. J. J. & Lloyd-Jones, G. C. Transmetalation in the Suzuki–Miyaura coupling: the fork in the trail. Angew. Chem. Int. Ed. 52, 7362–7370 (2013).
4. Cox, P. A. et al. Base-catalyzed aryl-B(OH)2 protodeboronation revisited: from concerted proton transfer to liberation of a transient aryl anion. J. Am. Chem. Soc. 139, 13156–13165 (2017).
5. Cox, P. A., Leach, A. G., Campbell, A. D. & Lloyd-Jones, G. C. Protodeboronation of heteroaromatic, vinyl, cyclopropyl boronic acids: pH–rate profiles, autocatalysis, and disproportionation. J. Am. Chem. Soc. 138, 9145–9157 (2016).
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