Chemistry in flow systems

Scholarly Works

• Yaghy, G.; Tonge, A.; Abouhakim, H.; Peeling, R.; Talford, M.; O'Brien, L.; Paksy, A.; Nevitt, P.; Muller, F.; Hanson, B.; Hunter, T. Opportunities for process intensification technologies in nuclear effluent treatment: A review of precipitators, adsorbers and separators. Chemical Engineering and Processing - Process Intensification 2023, 191, 109441. doi:10.1016/j.cep.2023.109441
• Ishitani, H.; Saito, Y.; Kobayashi, S. doi:10.1002/9781119736424.ch22
• Rehbein, M. C.; Guschakowski, M.; Sauter, W.; Kunz, J.; Schröder, U.; Scholl, S. Liquid–Liquid Equilibrium Data and Continuous Process Concept for the Electrosynthesis of Valeric Acid from Levulinic Acid. Frontiers in Energy Research 2020, 8. doi:10.3389/fenrg.2020.565570
• Myachin, I. V.; Orlova, A. V.; Kononov, L. O. Glycosylation in flow: effect of the flow rate and type of the mixer. Russian Chemical Bulletin 2019, 68, 2126–2129. doi:10.1007/s11172-019-2677-y
• Loponov, K. N.; Deadman, B. J.; Zhu, J.; Rielly, C. D.; Holdich, R.; Hii, K.; Hellgardt, K. Controlled multiphase oxidations for continuous manufacturing of fine chemicals. Chemical Engineering Journal 2017, 329, 220–230. doi:10.1016/j.cej.2017.05.017
• Wang, H.; Mustaffar, A.; Phan, A. N.; Zivkovic, V.; Reay, D.; Law, R.; Boodhoo, K. A review of process intensification applied to solids handling. Chemical Engineering and Processing: Process Intensification 2017, 118, 78–107. doi:10.1016/j.cep.2017.04.007
• Heitmann, D. Continuous and Intensified Laboratory Process Development at Clariant. Chemical Engineering & Technology 2016, 39, 1993–1995. doi:10.1002/ceat.201600150
• Bergami, M.; Protti, S.; Ravelli, D.; Fagnoni, M. Flow Metal-Free ArC Bond Formation via Photogenerated Phenyl Cations. Advanced Synthesis & Catalysis 2016, 358, 1164–1172. doi:10.1002/adsc.201600019
• Kononov, L. O. Chemical reactivity and solution structure: on the way to a paradigm shift?. RSC Advances 2015, 5, 46718–46734. doi:10.1039/c4ra17257d
• Kirschning, A. Chemistry in flow systems III. Beilstein journal of organic chemistry 2013, 9, 1696–1697. doi:10.3762/bjoc.9.193
• Ley, S. V.; Ingham, R. J.; O'Brien, M.; Browne, D. L. Camera-enabled techniques for organic synthesis. Beilstein journal of organic chemistry 2013, 9, 1051–1072. doi:10.3762/bjoc.9.118
• Pommella, A.; Tomaiuolo, G.; Chartoire, A.; Caserta, S.; Toscano, G.; Nolan, S. P.; Guido, S. Palladium-N-heterocyclic carbene (NHC) catalyzed C–N bond formation in a continuous flow microreactor. Effect of process parameters and comparison with batch operation. Chemical Engineering Journal 2013, 223, 578–583. doi:10.1016/j.cej.2013.03.070
• Czaban, J.; Torborg, C.; Grela, K. Sustainable Catalysis; Wiley, 2013; pp 163–214. doi:10.1002/9781118354520.ch09
• Šterk, D.; Jukič, M.; Časar, Z. Application of Flow Photochemical Bromination in the Synthesis of a 5-Bromomethylpyrimidine Precursor of Rosuvastatin: Improvement of Productivity and Product Purity. Organic Process Research & Development 2013, 17, 145–151. doi:10.1021/op300248y
• Baxendale, I. R.; Brocken, L.; Mallia, C. J. Flow chemistry approaches directed at improving chemical synthesis. Green Processing and Synthesis 2013, 2, 211–230. doi:10.1515/gps-2013-0029
• Hessel, V.; Noël, T. Ullmann's Encyclopedia of Industrial Chemistry; Wiley, 2012. doi:10.1002/14356007.q16_q01
• Hu, D. X.; O'Brien, M.; Ley, S. V. Continuous multiple liquid-liquid separation: diazotization of amino acids in flow. Organic letters 2012, 14, 4246–4249. doi:10.1021/ol301930h
• Rueping, M.; Bootwicha, T.; Sugiono, E. Continuous-flow catalytic asymmetric hydrogenations: Reaction optimization using FTIR inline analysis. Beilstein journal of organic chemistry 2012, 8, 300–307. doi:10.3762/bjoc.8.32
• Rueping, M.; Bootwicha, T.; Baars, H.; Sugiono, E. Continuous-flow hydration–condensation reaction: Synthesis of α,β-unsaturated ketones from alkynes and aldehydes by using a heterogeneous solid acid catalyst. Beilstein journal of organic chemistry 2011, 7, 1680–1687. doi:10.3762/bjoc.7.198
• Cambeiro, X. C.; Martín-Rapún, R.; Miranda, P. O.; Sayalero, S.; Alza, E.; Llanes, P.; Pericàs, M. A. Continuous-flow enantioselective α-aminoxylation of aldehydes catalyzed by a polystyrene-immobilized hydroxyproline. Beilstein journal of organic chemistry 2011, 7, 1486–1493. doi:10.3762/bjoc.7.172

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