Iron-catalysed substrate-directed Suzuki biaryl cross-coupling
Author:
Publisher
Springer Science and Business Media LLC
Subject
Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis
Link
http://www.nature.com/articles/s41929-018-0081-x.pdf
Reference57 articles.
1. Miyaura, N. & Suzuki, A. Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev. 95, 2457–2483 (1995).
2. Valente, C. & Organ, M. G. in Boronic Acids (ed. Hall, D. G.) 213–262 (Wiley, Weinheim, 2011).
3. Torborg, C. & Beller, M. Recent applications of palladium-catalyzed coupling reactions in the pharmaceutical, agrochemical, and fine chemical industries. Adv. Synth. Catal. 351, 3027–3043 (2009).
4. Garrett, C. E. & Prasad, K. The art of meeting palladium specifications in active pharmaceutical ingredients produced by Pd-catalyzed reactions. Adv. Synth. Catal. 346, 889–900 (2004).
5. Han, F.-S. Transition-metal-catalyzed Suzuki–Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts. Chem. Soc. Rev. 42, 5270–5298 (2013).
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