10 Intermolecular Transition-Metal-Catalyzed C—C Coupling Reactions in Continuous Flow
Buch
Herausgeber: Jamison, T. F.; Koch, G.
Titel: Flow Chemistry in Organic Synthesis
Print ISBN: 9783132423312; Online ISBN: 9783132423350; Buch-DOI: 10.1055/b-006-161272
1st edition © 2018. Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart
Fachgebiete: Organische Chemie;Chemische Reaktionen, Katalyse;Organometallchemie;Chemische Labormethoden, Stöchiometrie
Science of Synthesis Reference Libraries
Übergeordnete Publikation
Titel: Science of Synthesis
DOI: 10.1055/b-00000101
Reihenherausgeber: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.
Typ: Mehrbändiges Werk
Abstract
This chapter provides an up-to-date collection of prominent examples of intermolecular transition-metal-catalyzed C–C coupling reactions performed in continuous-flow systems. The advantages offered by flow technology for the implementation of traditional cross-coupling methods are discussed. Moreover, recent examples of the successful application of flow reactors for C–H functionalization strategies (including C–H activation and dual photoredox transition-metal catalysis) are reviewed.
Schlüsselwörter
transition-metal catalysis - cross coupling - Suzuki–Miyaura coupling - Negishi coupling - Mizoroki–Heck coupling - carbonylative coupling - continuous flow - C–H functionalization - dehydrogenative coupling - C–H activation - dual catalysis- 2 Metal-Catalyzed Cross-Coupling Reactions. de Meijere A, Diederich F. Wiley-VCH; Weinheim, Germany 2004
- 5 Anastas PT, Warner JC. Green Chemistry: Theory and Practice. Oxford University Press; Oxford, UK 1998
- 20 Noël T, Hessel V, In: New Trends in Cross-Coupling: Theory and Applications Colacot TJ. Royal Society of Chemistry Cambridge, UK 2015; 610-644
- 25 Dalla-Vechia L, Reichart B, Glasnov T, Miranda LSM, Kappe CO, de Souza ROMA. Org. Biomol. Chem. 2013; 11: 6806
- 28 Theberge AB, Whyte G, Frenzel M, Fidalgo LM, Wootton RCR, Huck WTS. Chem. Commun. (Cambridge) 2009; 6225
- 40 Beller M, Wu X.-F. Transition Metal Catalyzed Carbonylation Reactions. Springer; Heidelberg 2013: 133-146
- 41 Miller PW, Long NJ, de Mello AJ, Vilar R, Passchier J, Gee A. Chem. Commun. (Cambridge) 2006; 546
- 42 Miller PW, Long NJ, de Mello AJ, Vilar R, Audrain H, Bender D, Passchier J, Gee A. Angew. Chem. Int. Ed. 2007; 46: 2875
- 47 Laudadio G, Noël T, In: Strategies for Palladium-Catalyzed Non-Directed and Directed C-H Bond Functionalization Kapdi AR, Maiti D. Elsevier Amsterdam 2017; 275-288
- 58 Ferreira EM, Zhang H, Stoltz BM, In: The Mizoroki-Heck Reaction Oestreich M. Wiley Chichester, UK 2009; 345-382
- 61 Wang H, Pesciaioli F, Oliveira JCA, Warratz S, Ackermann L. Angew. Chem. Int. Ed. 2017; 56: 15063
- 73 Tellis JC, Kelly CB, Primer DN, Jouffroy M, Patel NR, Molander GA. Acc. Chem. Res. 2016; 49: 1429
- 75 Welin ER, Le C, Arias-Rotondo DM, McCusker JK, MacMillan DWC. Science (Washington, D. C.) 2017; 355: 380
- 80 Zuo Z, Ahneman DT, Chu L, Terrett JA, Doyle AG, MacMillan DWC. Science (Washington, D. C.) 2014; 345: 437