ThalesNano has set a new standard for laboratory-scale continuous flow reactions, especially on the field of hydrogenation. Our instruments have been used all around the world for a wide range of applications and have been featured in numerous scientific publications.
Browse our poblications in alphabetical order below, filter by catalyst, device, industry or reaction type, or download the complete list.
1,3,5-Trisubstituted pyrazoles as potent negative allosteric modulators of the mGlu2/3 receptors
Van Gool, M.; Alonso De Diego, S. A.; Delgado, O.; Trabanco, A. A.; Jourdan, F.; Macdonald, G. J.; Somers, M.; Ver Donck, L.; ChemMedChem, 2017, 12(12), 905-912
1,8-Naphthalimide derivatives: new leads against dynamin I GTPase activity
Abdel-Hamid, M. K.; Macgregor, K. A.; Odell, L. R.; Chau, N.; Mariana, A.; Whiting, A.; Robinson, P. J.; McCluskey, A.; Org. Biomol. Chem., 2015, 13, 8016-8028
2,7-Pyrrolo[2,1-f][1,2,4]triazines as JAK2 inhibitors: modification of target structure to minimize reactive metabolite formation
Weinberg, L. R.; Albom, M. S.; Angeles, T. S.; Breslin, H. J.; Gingrich, D. E.; Huang, Z.; Lisko, J. G.; Mason, J. L.; Milkiewicz, K. L.; Thieu, T. V.; Underiner, T.L .; Wells, G. J.; Wells-Knecht, K. J.; Dorsey, B. D.; Bioorg. Med. Chem. Lett., 2011, 21(4), 7325-7330
Link to article3‐Aminoazetidin‐2‐one derivatives as N‐acylethanolamine acid amidase (NAAA) inhibitors suitable for systemic administration
Fiasella, A.; Nuzzi, A.; Summa, M.; Armirotti, A.; Tarozzo, G.; Tarzia, G.; Mor, M.; Bertozzi, F.; Bandiera, T.; Piomelli, D.; ChemMedChem, 2014, 9(7), 1602-1614
3-(Oxazolo[4,5-b]pyridin-2-yl)anilides as a novel class of potent inhibitors for the kinetoplastid Trypanosoma brucei, the causative agent for human African trypanosomiasis
Ferrins, L.; Rahmani, R.; Sykes, M. L.; Jones, A. J.; Avery, V. M.; Teston, E.; Almohaywi, B.; Yin, J.; Smith, J.; Hyland, C.; White, K. L.; Ryan, E.; Campbell, M.; Charman, S. A.; Kaiser, M.; Baell, J. B.; Eur. J. Med. Chem., 2013, 66, 450-465
3-Substituted xanthines as promising candidates for quadruplex formation: computational, synthetic and analytical studies
Szolomajer, J.; Paragi, G.; Batta, Gy.; Guerra, F. C.; Bickelhaupt, F. M.; Kele, Z.; Padar, P.; Kupihar, Z.; Kovacs, L.; New Journal of Chemistry, 2011, 35, 476-482
4-(3-Aminoazetidin-1-yl)pyrimidin-2-amines as high-affinity non-imidazole histamine H3 receptor agonists with in vivo central nervous system activity
Wagner, G.; Mocking, T.; Arimont, M.; Provensi, G.; Rani, B.; Silva-Marques, B.; Latacz, G.; Da Costa Pereira, D.; Karatzidou, K.; Vischer, H. F.; Wijtmans, M.; Kiec-Kononowicz, K.; De Esch, I. J. P.; Leurs, R.; J. Med. Chem., 2019, accepted manuscript
4′-C-methyl-2-deoxyadenosine and 4-C-ethyl-2-deoxyadenosine inhibit HIV-1 replication
Vu, B. C.; Boyer, P. L.; Siddiqui, M. A.; Marquez, V. E.; Hughes, S. H.; Antimicrobial Agents and Chemotheraphy, 2011, 55(5), 2379-2389
4-Methyl-6,7-dihydro-4H-triazolo[4,5-c]pyridine-based P2X7 receptor antagonists: optimization of pharmacokinetic properties leading to the identification of a clinical candidate
Letavic, M. A.; Savall, B. M.; Allison, B. D.; Aluisio, L.; Andres, J. I.; De Angelis, M.; Ao, H.; Beauchamp, D. A.; Bonaventure, P.; Bryant, S.; Carruthers, N. I.; Ceusters, M.; Coe, K. J.; Dvorak, C. A.; Fraser, I. C.; Gelin, C. F.; Koudriakova, T.; Liang, J.; Lord, B.; Lovenberg, T. W.; Otieno, M. A.; Schoetens, F.; Swanson, D. M.; Wang, Q.; Wickenden, A. D.; Bhattacharya, A.; J. Med. Chem., 2017, 60(11), 4559-4572
Synthesis, antiplasmodial activity and in silico molecular docking study of pinocembrin and its analogs
Melaku, Y. et al.; BMC Chemistry, 2022, 16:36
Synthesis of 12β-methyl-18-nor-avicholic acid analogues as potential TGR5 agonists
Ure, E. M. et al.; Org. Biomol. Chem., 2022, 20, 3511-3527
α-1,4-Galactosyltransferase-catalyzed glycosylation of sugar and lipid modified Leu-enkephalins
Simerska, P.; Christie, M. P.; Goodwin, D.; Jen, F. E-C.; Jennings, M. P.; Toth, I.; Journal of Molecular Catalysis B: Enzymatic, 2013, 97, 196-202
A benchtop continuous flow reactor: a solution to the hazards posed by gas cylinder based hydrogenation
Dorman, G.; Kocsis, L.; Jones, R.; Darvas, F.; Journal of Chemical Health and Safety, 2013, 20(4), 3-8
A comparative assessment study of known small-molecule Keap1−Nrf2 protein–protein interaction inhibitors: Chemical synthesis, binding properties, and cellular activity
Tran, K. T.; Pallesen, J. S.; Solbak, S. M. O.; Narayanan, D.; Baig, A.; Zang, J.; Aguayo-Orozco, A.; Carmona, R. M. C.; Garcia, A. D.; Bach, A.; J. Med. Chem., 2019, 62(17), 8028-8052
A comprehensive review of flow chemistry techniques tailored to the flavours and fragrances industries
Gambarcorta, G. et al.; Beilstein J. Org. Chem., 2021, 17, 1181-1312
A concise flow synthesis of indole-3-carboxylic ester and its derivatisation to an auxin mimic
Baumann, M.; Baxendale, I. R.; Deplante, F.; Beilstein J. Org. Chem., 2017, 13, 2549-2560
A concise stereoselective synthesis of pterosin B
Dexter, H. R.; Allen, E.; Williams, D. M.; Tetrahedron Letters, 2018, 59(49), 4323-4325
A continuous-flow approach to palladium-catalyzed alkoxycarbonylation reactions
Kelly, C. B.; Lee, C. (X.); Mercadante, M. A.; Leadbeater N. E.; Org. Process Res. Dev., 2011, 15(3), 717-720
A continuous-flow microwave reactor for conducting high-temperature and high-pressure chemical reactions
Sauks, J. M.; Mallik, D.; Lawryshyn, Y.; Bender, T.; Organ, M.; Org. Process Res. Dev., 2014, 18(11), 1310-1314
A continuous flow process for the green and sustainable production of N-alkyl imidazoles
Fekete, M.; Kocsis L.; Dorman, G.; Jones, R. V.; Darvas, F.; Green Processing and Synthesis, 2016, 5(3), 239-246
A continuous flow process for the production of 2,5-dimethylfuran from fructose using (non-noble metal based) heterogeneous catalysis
Braun, M.; Antonietti, M.; Green Chemistry, 2017, 19, 3813-3819
A continuous flow strategy for the facile synthesis and elaboration of semi-saturated heterobicyclic fragments
Luise, N.; Wyatt, E. W.; Tarver, G. J.; Wyatt, P. G.; Eur. J. Org. Chem., 2018, 2019(6), 1341-1349
A continuous-flow synthesis of 1,4-benzodiazepin-5-ones, privileged scaffolds for drug discovery
Viviano, M.; Milite, C.; Rescigno, D.; Castellano, S.; Sbardella, G.; RSC Adv., 2015, 5, 1268-1273
A continuous flow system for asymmetric hydrogenation using supported chiral catalysts
Madarasz, J.; Farkas, G.; Balogh, S.; Szollosy, A.; Kovacs, J.; Darvas, F.; Urge, L.; Bakos, J.; J. Flow Chem., 2011, 1(2), 62-67
A continuous-flow, two-step, metal-free process for the synthesis of differently substituted chiral 1,2-diamino derivatives
Pirola, M.; Compostella, M. E.; Raimondi, L.; Puglisi, A.; Benaglia, M.; Synthesis, 2018, 50, 1430-1438
A continuous process for glyoxal valorisation using tailored Lewis-acid zeolite catalysts
Dapsens, P. Y.; Mondelli, C.; Kusema, B. T.; Verel, R., Perez-Ramirez, J.; Green Chemistry, 2014, 16, 1176-1186
A Continuous‐Flow Process for Palladium‐Catalyzed Olefin Cleavage by using Oxygen within the Explosive Regime
Hone, C. A. et al.; ChemCatChem, 2017, 9, 3298-3302
A convenient total synthesis of PSMA-617: A prostate specific membrane antigen (PSMA) ligand for prostate cancer endotherapeutic applications
Kumar, K. S. A. et al.; Eur. J. Med. Chem. Rep., 2022, 6, 100084
A Facile hybrid ‘flow and batch’ access to substituted 3,4-dihydro-2H-benzo[b][1,4]oxazinones
Lin, A. J. S. et al.; Org. Biomol. Chem., 2016, 14, 8732-8742
A facile, protic ionic liquid route to N-substituted 5-hydroxy-4-methyl-3-oxoisoindoline-1-carboxamides and N-substituted 3-oxoisoindoline-4-carboxylic acids
Gordon, C. P.; Byrne, N.; McCluskey, A.; Green Chem., 2010, 12, 1000-1006
A flexible approach to 6,5-benzannulated spiroketals
Wilson, Z. E.; Hubert, J. G.; Brimble, M. A.; Eur. J. Org. Chem., 2011, 2011(20-21), 3938-3945
A flexible synthesis of C-6 and N-1 analogues of a 4-amino-1,3-dihydroimidazo[4,5-c]pyridin-2-one core
Hay, D. A.; Adam, F. M.; Bish, G.; Calo, F.; Dixon, R.; Fray, M. J.; Hitchin, J.; Jones, P.; Paradowski, M.; Parsons, G. C.; Proctor, K. J. W.; Pryde, D. C.; Smith, N. N.; Tran, T. D.; Tetrahedron Letters, 2011, 52(44), 5728-5732
A flow-based synthesis of telmisartan
Martin, A. D.; Siamaki, A. R.; Belecki, K.; Gupton, B. F.; J. Flow Chem., 2015, 5(3), 145-147
A flow-based transition-metal-catalysed hydrogenolysis strategy to facilitate peptide side-chain deprotection
Menti-Platten, M. et al.; Org. Biomol. Chem., 2022, 20, 106-112
A flow chemistry route to 2-phenyl-3-(1H-pyrrol-2-yl)propan-1-amines
Tarleton, M.; McCluskey, A.; Tetrahedron Letters, 2011, 52(14), 1583-1586
A flow process for the multi-step synthesis of the alkaloid natural product oxomaritidine: a new paradigm for molecular assembly
Baxendale, I. R.; Deeley, J.; Griffiths-Jones, C. M.; Ley, S. V.; Saaby, S.; Tranmer, G. K.; Chem. Commun., 2006, 2566-2568
A flow process using microreactors for the preparation of a quinolone derivative as a potent 5HT1B antagonist
Qian, Z.; Baxendale, I. R.; Ley, S. V.; Synlett, 2010, 4, 505-508
A flow reactor process for the synthesis of peptides utilizing immobilized reagents, scavengers and catch and release protocols
Baxendale, I. R.; Ley, S. V.; Smith, C. D.; Tranmer, G. K.; Chem. Commun., 2006, 4835-4837
A gram-scale batch and flow total synthesis of perhydrohistrionicotoxin
Brasholz, M.; Macdonald, J. M.; Saubern, S.; Ryan, J. H.; Holmes, A. B.; Chem. Eur. J., 2010, 16(37), 11471-11480
A Green Process for the Preparation of Bis(2,2,2-trifluoroethyl) Methylphosphonate
Molnar, K. et al.; Org. Process Res. Dev., 2017, 21, 1985-1989
A method to identify best available technologies (BAT) for hydrogenation reactors in the pharmaceutical industry
Van Le Doan, T.; Stavarek, P.; de Bellefon, C.; J. Flow Chem., 2012, 2(3), 77-82
A modular synthesis of teraryl‐based α‐helix mimetics, part 2: Synthesis of 5‐pyridine boronic acid pinacol ester building blocks with amino acid side chains in 3‐position
Peters, M.; Trobe, M.; Breinbauer, R.; Chem. Eur. J., 2013, 19(7), 2450-2456
A multi-step continuous flow synthesis of pomalidomide
Ivanova, M. et al.; J. Flow Chem., 2022, https://doi.org/10.1007/s41981-022-00223-3
A multistep continuous-flow system for rapid on-demand synthesis of receptor ligands
Petersen, T. P.; Ritzen, A.; Ulven, T.; Org. Lett., 2009, 11(22), 5134-5137
A novel agonist of the type 1 lysophosphatidic acid receptor (LPA1), UCM-05194, shows efficacy in neuropathic pain amelioration
Gonzalez Gil, I.; Zian, D.; Vazquez-Villa, H.; Hernandez-Torres, G.; Martinez, R. F.; Khiar-Fernandez, N.; Rivera, R.; Kihara, Y.; Devesa, I.; Mathivanan, S.; Rosell del Valle, C.; Zambrana-Infantes, E.; Puigdomenech, M.; Cincilla, G.; Sanchez-Martinez, M.; Rodriguez de Fonseca, F.; Ferrer-Montiel, A.; Chun, J.; Lopez-Vales, R.; Lopez-Rodriguez, M. L.; Ortega-Gutierrez, S.; J. med. Chem., 2019, accepted manuscript
A novel aminothiazole KY-05009 with potential to inhibit Traf2- and Nck-interacting kinase (TNIK) attenuates TGF-β1-mediated epithelial-to-mesenchymal transition in human lung adenocarcinoma A549 cells
Kim, J.; Moon, S. H.; Kim, B. T.; Chae, C. H.; Lee, J. Y.; Kim, S. H.; PLoS One, 2014, 9(10), e110180
A novel method for high-throughput reduction of compounds through automated sequential injection into a continuous-flow microfluidic reactor
Jones, R.; Godorhazy, L.; Szalay, D.; Gerencser, J.; Dorman, G.; Urge, L.; Darvas, F.; QSAR Comb. Sci., 2005, 24(6), 722-727
A practical and benign synthesis of amines through Pd@mpg-C3N4 catalyzed reduction of nitriles
Li, Y.; Gong, Y.; Xu, X.; Zhang, P.; Li, H.; Wang, Y.; Catalysis Communications, 2012, 28, 9-12
A remote-controlled adaptive medchem lab: an innovative approach to enable drug discovery in the 21st Century
Godfrey, A. G.; Masquelin, T.; Hemmerle, H.; Drug Discovery Today, 2013, 18(17-18), 795-802
A safe and selective method for reduction of 2-nitrophenylacetic acid systems to N-aryl hydroxamic acids using continuous flow hydrogenation
Ichire, O.; Jans, P.; Parfenov, G.; Dounay, A. B.; Tetrahedron Letters, 2017, 58(6), 582-585
A scalable two-step continuous flow synthesis of nabumetone and related 4-aryl-2-butanones
Viviano, M.; Glasnov, T. N.; Reichard, B.; Tekautz, B.; Kappe, C. O.; Org. Process Res. Dev., 2011, 15, 858-870
A simple chemical model for clathrate hydrate inhibition by polyvinylcaprolactam
Davenport, J. R.; Musa, O. M.; Paterson, M. J.; Piepenbrock, M. O. M.; Fucke, K.; Steed, J. W.; Chem. Commun., 2011, 47, 9891-9893
A simple, efficient, and selective deuteration via a flow chemistry approach
Mandity, I. M.; Martinek, T. A.; Darvas, F.; Fulop, F.; Tetrahedron Letters, 2009, 50, 4372-4374
A small footprint oxycodone generator based on continuous flow technology and real-time analytics
Sommer, F. et al.; J. Flow Chem., 2021, 11, 707-715
A stereoselective, catalytic strategy for the in-flow synthesis of advanced precursors of rasagiline and tamsulosin
Brenna, D.; Pirola, M.; Raimondi, L.; Burke, A. J.; Benaglia, M.; Bioorg. Med. Chem., 2017, 25(23), 6242-6247
A structure-based design approach to advance the allyltyrosine-based series of HIV integrase inhibitors
Gordon, C. P.; Dalton, N.; Vandegraaff N.; Deadman, J.; Rhodes, D. I.; Coates, J. A.; Pyne, S. G.; Griffith, R.; Bremner, J. B.; Keller, P. A.; Tetrahedron, 2018, 74(12), 1253-1268
A sustainable and chemoselective continuous flow hydrogenation of functionalized 2-azetines to azetidines
Graziano, E. et al.; Tetrahedron Green Chem., 2023, 1, 100003
A three step continuous flow synthesis of the biaryl unit of the HIV protease inhibitor Atazanavir
Dalla-Vechia, L.; Reichart, B.; Glasnov, T. N.; Miranda, L. S. M.; Kappe, C. O.; de Souza, R. O. M. A.; Org. Biomol. Chem., 2013, 11, 6806-6813
A ‘turn-on’ fluorescence glycosyl dithiocarbamate probe for selective fluoride sensing in aqueous medium
Das, R.; Mishra, B.; Mukhopadhyay, B.; Synlett, 2018, 29(15), 2001-2005
A two‐step continuous‐flow synthesis of N‐(2‐aminoethyl)acylamides through ring‐opening/hydrogenation of oxazolines
Gutmann, B.; Roduit, J. P.; Roberge, D.; Kappe, C. O.; Chem. Eur. J., 2011, 17, 13146-13150
A versatile biobased continuous flow strategy for the production of 3-butene-1,2-diol and vinyl ethylene carbonate from erythritol
Tshibalonza, N. N.; Gerardy, R.; Alsafra, Z.; Eppe, G.; Monbaliu, J-C. M.; Green Chem., 2018, 20, 5147-5157
A versatile de novo synthesis of legionaminic acid and 4-epi-legionaminic acid starting from D-serine
Gintner, M.; Yoneda, Y.; Schmölzer, C.; Denner, C.; Kahlig, H.; Schmid, W.; Carbohydrate Research, 2019, 474, 34-42
A Warburg effect targeting vector designed to increase the uptake of compounds by cancer cells demonstrates glucose and hypoxia dependent uptake
Glenister, A.; Simone, M. I.; Hambley, T. W.; PLos One, 2019, online article
Access to optically active 3‐aminopiperidines by ring expansion of prolinols: Thermodynamic versus kinetic control
Cochi, A. ; Pardo, D. G.; Cossy, J.; Eur. J. Org. Chem., 2012, 2012(10), 2023-2040
Accessing novel process windows in a high‐temperature/pressure capillary flow reactor
Razzaq, T.; Glasnov, T. N.; Kappe, C. O.; Chem. Eng. Technol., 2009, 32(11), 1702-1716
Activity of continuous flow synthesized Pd-based nanocatalysts in the flow hydroconversion of furfural
Garcia-Olmo, A. J.; Yepez, A.; Balu, A. M.; Prinsen, P.; Garcia, A.; Maziere, A.; Len, C.; Luque, R.; Tetrahedrom, 2017, 73(38), 5599-5604
Acylguanidine beta secretase 1 inhibitors: a combined experimental and free energy perturbation study
Keranen, H.; Perez-Benito, L.; Ciordia, M.; Delgado, F.; Steinbrecher, T. B.; Oehlrich, D.; van Vlijmen, H. W. T.; Trabanco, A. A.; Tresadern, G.; J. Chem. Theory Comput., 2017, 13, 1439-1453
Adaptive and automated system-optimization for heterogeneous flow-hydrogenation reactions
Fabry, D. C.; Heddrich, S.; Sugiono, E.; Liauw, M. A.; Rueping, M.; React. Chem. Eng., 2019, 4, 1486-1491
Additive manufacturing technologies: 3D printing in organic synthesis
Rossi, S.; Puglisi, A.; Banglia, M.; ChemCatChem, 2018, 10(7), 1512-1525
Advanced Real-Time Process Analyticsfor Multistep Synthesis in Continuous Flow
Sagmeister, P. et al.; Angew. Chem. Int. Ed., 2021, 60, 8139-8148
Aerobic flow oxidation of alcohols in water catalyzed by platinum nanoparticles dispersed in an amphiphilic polymer
Osako, T.; Torii, K.; Uozumi, Y.; RSC Adv., 2015, 5, 2647-2654
Aerobic oxidations in flow: opportunities for the fine chemicals and pharmaceuticals industries
Gavriilidis, A. et al.; React. Chem. Eng., 2016, 1, 595-612
Alkyne–azide cycloadditions with copper powder in a high‐pressure continuous‐flow reactor: High‐temperature conditions versus the role of additives
Otvos, S. B.; Mandity, I. M.; Kiss, L.; Fulop, F.; Chem. Asian J., 2013, 8(4), 800-808
Aminoadamantanes containing monoterpene-derived fragments as potent tyrosyl-DNA phosphodiesterase 1 inhibitor
Ponomarev, K. Yu.; Suslov, E. V.; Zakharenko, A. L.; Zakharova, O. D.; Rogachev, A. D.; Korchagina, D. V.; Zafar, A.; Reynisson, J.; Nefedov, A. A.; Volcho, K. P.; Salakhutdinov, N. F.; Lavrik, O. I.; Bioorg. Chem., 2018, 76, 392-399
Aminopyrazine inhibitors binding to an unusual inactive conformation of the mitotic kinase Nek2: SAR and structural characterization
Whelligan, D. K.; Solanki, S.; Taylor, D.; Thomson, D. W.; Cheung, K. J.; Boxall, K.; Mas-Droux, C.; Barillari, C.; Burns, S.; Grummitt, C. G.; Collins, I.; van Montfort, E. L. M.; Aherne, G. W.; Bayliss, R.; Hoelder, S.; J. Med. Chem., 2010, 53, 7682-7698
An alternative route for fondaparinux sodium synthesis via selective hydrogenations and sulfation of appropriate pentasaccharides
Manikowski, A.; Koziol, A.; Czajkowska-Wojciechowska, E.; Carbohydrate Research, 2012, 361, 155-161
An efficient and more sustainable one-step continuous-flow multicomponent synthesis approach to chromene derivatives
Vaddula, B. R.; Yalla, S.; Gonzalez, M. A.; J. Flow Chem., 2015, 5(3), 172-177
An efficient and transition metal free protocol for the transfer hydrogenation of ketones as a continuous flow process
Sedelmeier, J.; Ley, S. V.; Baxendale, I. R.; Green Chem., 2009, 11, 683-685
An efficient continuous flow approach to furnish furan-based biaryls
Trinh, T. N.; Hizartzidis, L.; Lin, A. J. S.; Harman, D. G.; McCluskey, A.; Gordon, C. P.; Org. Biomol. Chem., 2014, 12, 9562-9571
An imidazolium-based organopalladium-functionalized organic–inorganic hybrid silica promotes one-pot tandem Suzuki cross coupling–reduction of haloacetophenones and arylboronic acids
Zhang, D.; Cheng, T.; Liu, G.; Applied Catal. B: Environmental, 2015, 174-175, 344-349
An Integrated Continuous-Flow Synthesis of a Key Oxazolidine Intermediate to Noroxymorphone from Naturally Occurring Opioids
Mata, A. et al.; Eur. J. Org. Chem., 2017, 6505-6510
An integrated flow and microwave approach to a broad spectrum protein kinase inhibitor
Russell, C.; Lin, A. J. S.; Hains, P.; Simone, M. I.; Robinson, P. J.; McCluskey, A.; RSC Adv., 2015, 5, 93433-93437
An orally bioavailable, indole-3-glyoxylamide based series of tubulin polymerization inhibitors showing tumor growth inhibition in a mouse xenograft model of head and neck cancer
Colley, H. E.; Muthana, M.; Danson, J. S.; Jackson, L. V.; Brett, M. L.; Harrison, J.; Coole, S. F.; Mason, D. P.; Jennings, L. R.; Wong, M.; Tulasi, V.; Noraman, D.; Lockey, P. M.; Williams, L.; Dossetter, A. G.; Griffen, E. J.; Thompson, M. J.; J. Med. Chem., 2015, 58(23), 9309-9333
Application of continuous flow and alternative energy devices for 5-hydroxymethylfurfural production
Schon, M.; Schnurch, M.; Mihovilovic, M. D.; Mol. Divers., 2011, 15, 639-643
Application of deuterated THENA for assigning the absolute configuration of chiral secondary alcohols
Soponpong, J.; Dolsophon, K.; Thongpanchang, C.; Linden, A.; Thongpanchang, T.; Tetrahedron Letters, 2019, 60(6), 497-500
Application of factorial design of experiments for the continuous hydrogenation of enriched castor oil methyl esters
Neeharika, T. S. V. R.; Rani, K. N. P.; Rao, K. V. S. A.; Kumar, T. P.; Prasad, R. B. N.; Bulletin of Chemical Reaction Engineering & Catalysis, 2013, 8(2), 154-159
Application of metal‐based reagents and catalysts in microstructured flow devices
Chinnusamy, T.; Yudha S. S.; Hager, M.; Kreitmeier, P.; Reisen, O.; ChemSusChem, 2012, 5(2), 247-255
Applying flow chemistry: Methods, materials, and multistep synthesis
McQuade, D. T.; Seeberger, P. H.; J. Org. Chem., 2013, 78(13), 6384-6389
Approaches for Performing Reductions under Continuous-Flow Conditions
Neyt, N. C. et al.; Synthesis, 2018, 50(14), 2707-2720
Approaches to pyranuronic β-sugar amino acid building blocks of peptidosaccharide foldamers
Goldschmidt-Goz, V.; Pinter, I.; Harmat, V.; Perczel, A.; Eur. J. Org. Chem., 2018, 3, 355-361
Aqueous flow hydroxycarbonylation of aryl halides catalyzed by an amphiphilic polymer-supported palladium–diphenylphosphine catalyst
Osako, T.; Kaiser, R.; Torii, K.; Uozumi, Y.; Synlett, 2019, 30, 961-966
Assessing a sustainable manufacturing route to lapatinib
Stark, R. T. et al.; React. Chem. Eng., 2022, Advance article
Assignment of vibrational circular dichroism cross‐referenced electronic circular dichroism spectra of flexible foldamer building blocks: Towards assigning pure chiroptical properties of foldamers
Farkas, V.; Nagy, A.; Menyhard, D. K.; Perczel, A.; Chem. Eur. J., 2019, 25(65), 14890-14900
Asymmetric aldol reaction in a continuous-flow reactor catalyzed by a highly reusable heterogeneous peptide
Otvos, S. B.; Mandity, I. M.; Fulop, F.; J. Cat., 2012, 295, 179-185
Asymmetric hydrogenation of C=C double bonds using Rh-complex under homogeneous, heterogeneous and continuous mode conditions
Balogh S.; Farkas, G.; Madarasz, J.; Szollosy, A.; Kovacs, J.; Darvas, F.; Urge L.; Bakos, J.; Green Chem., 2012, 14, 1146-1151
Asymmetric Mannich reaction of dicarbonyl compounds with α-amido sulfones catalyzed by cinchona alkaloids and synthesis of chiral dihydropyrimidones
Lou, S.; Dai, P.; Schaus, S. E.; J. Org. Chem., 2007, 72, 9998-10008
Asymmetric organocatalytic Michael addition–cyclisation cascade of cyclopentane-1,2-dione with alkylidene malononitriles
Silm, E.; Kaabel, S.; Jarving, I.; Kanger, T.; Synthesis, 2019, 51, 4198-4204
Asymmetric Synthesis of γ-Amino-Functionalised Vinyl Sulfones: De Novo Preparation of Cysteine Protease Inhibitors
Shen, W. et al.; Synthesis, 2022, 54(7), 1753-1764
Asymmetric Synthesis of Trisubstituted Piperidines via Biocatalytic Transamination and Diastereoselective Enamine or Imine Reduction
Petermeier, P. et al.; Adv. Synth. Catal., 2023, Early view
Asymmetric Total Synthesis of (-)-Erogorgiaene and Its C-11 Epimer and Investigation of Their Antimycobacterial Activity
Incerti-Pradillos, C. A. et al.; Chem. Eur. J., 2016, 22, 14390-14396
Atomic Cu on nanodiamond-based sp2/sp3 hybrid nanostructures for selective hydrogenation of phenylacetylene
Sun, Y.; Luo, B.; Xu, S.; Guo, W.; Huang, X.; Shao, L.; Chemical Physics Letters, 2019, 723, 39-43
Automated and continuous synthesis of drug substances
Castillo, I. et al.; Chem. Eng. Res. Des., 2021, 177, 493-501
Automated flow and real-time analytics approach for screening functional group tolerance in heterogeneous catalytic reactions
Simon, K. et al.; Catal. Sci. Technol., 2022, 12, 1799-1811
Automated technology for performing flow chemistry at elevated temperature and pressure
Kovacs, I.; Jones, R. V.; Niesz, K.; Csajagi, Cs.; Borcsek, B.; Darvas, F.; Urge, L.; JALA, 2007, 12, 284-290
Autonomous continuous flow reactor synthesis for scalable atom-precision
Sumpter, B. G. et al.; Carbon Trends, 2023, 10, 100234
Aziridine ring opening for the synthesis of sphingolipid analogues: Inhibitors of sphingolipid-metabolizing enzymes
Alcaide, A.; Llebaria, A.; J. Org. Chem., 2014, 79(7), 2993-3029
Batch and continuous-flow room temperature furfural acetalization with ethanol over aluminophosphate (APAl) catalysts for biofuels production
Ratthiwal, J. et al.; Fuel, 2023, 332, 126049
Batch and flow hydrotreatment of water contaminated by trichloroethylene on active carbon supported nickel catalysts
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Flash carboxylation: fast lithiation-carboxylation sequence at room temperature in continuous flow
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Flow chemistry vs. flow analysis
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Fused bicyclic piperidines and dihydropyridines by dearomatising cyclisation
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Hazards associated with laboratory scale hydrogenations
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Hepatitis C virus NS5A replication complex inhibitors. Part 6: Discovery of a novel and highly potent biarylimidazole chemotype with inhibitory activity toward genotypes 1a and 1b replicons
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Highly efficient reversible addition-fragmentation chain‐transfer polymerization in ethanol/water via flow chemistry
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Highly efficient thermal cyclization reactions of alkylidene esters in continuous flow to give aromatic/heteroaromatic derivatives
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Hit optimization of 5-substituted-N-(piperidin-4-ylmethyl)-1H-indazole-3-carboxamides: Potent Glycogen Synthase Kinase-3 (GSK-3) inhibitors with in vivo activity in model of mood disorders
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HKUST-1 silica aerogel composites: novel materials for the separation of saturated and unsaturated hydrocarbons by conventional liquid chromatography
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How the mode of Candida antarctica lipase B immobilization affects the continuous-flow kinetic resolution of racemic amines at various temperatures
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Identification and Characterization of Carprofen as a Multitarget Fatty Acid Amide Hydrolase/Cyclooxygenase Inhibitor
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Identification and validation of small molecule modulators of the NusB-NusE interaction
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Identification of a novel orally bioavailable phosphodiesterase 10A inhibitor with efficacy in animal models of schizophrenia
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Identification of a Potent, Selective, and Brain-Penetrant Rho Kinase Inhibitor and its Activity in a Mouse Model of Huntington’s Disease
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Immobilized iron oxide nanoparticles as stable and reusable catalysts for hydrazine‐mediated nitro reductions in continuous flow
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Immobilized phosphine–phosphite rhodium complexes: highly active and enantioselective catalysts for asymmetric hydrogenation under continuous flow conditions
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Immobilized transition metals as catalysts for cross-couplings in continuous flow — A critical assessment of the reaction mechanism and metal leaching
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Important industrial procedures revisited in flow: very efficient oxidation and N-alkylation reactions with high atom-economy
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Improved and scalable synthesis of building blocks for the modular synthesis of teraryl-based alpha-helix mimetics
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Improved continuous flow processing: benzimidazole ring formation via catalytic hydrogenation of an aromatic nitro compound
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In vitro reconstitution guide for targeted synthetic metabolism of chemicals, nutraceuticals and drug precursors
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Increasing selectivity of CC chemokine receptor 8 antagonists by engineering nondesolvation related interactions with the intended and off-target binding sites
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Innovative benign-by-design flow chemistry protocols: from bio(nano)materials synthesis to biomass/waste valorisation
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Reissert indole synthesis using continuous-flow hydrogenation
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Scale-up of flow-assisted synthesis of C2-symmetric chiral PyBox ligands
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Scouting in silico different chemo-types of PDE4 inhibitors to guide the design of new anti-inflammatory/antioxidant agents
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Single-atom heterogeneous catalysts based on distinct carbon nitride scaffolds
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Site‐selective deuterated‐alkene synthesis with palladium on boron nitride
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Small-Molecule Inhibitors of the NusB−NusE Protein−Protein Interaction with Antibiotic Activity
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Ouchi, T.; Mutton, R. J.; Rojas, V.; Fitzpatrick, D. E.; Cork, D. G.; Battilocchio, C.; Ley, S. V.; ACS Sustainable Chem. Eng., 2016, 4, 1912-1916
Solvent-free enzymatic process for biolubricant production in continuous microfluidic reactor
Madarasz, J.; Nemeth, D.; Bakos, J.; Gubicza, L.; Bakonyi, P.; Journal of Cleaner Production, 2015, 93, 140-144
Sonogashira cross-coupling under non-basic conditions. Flow chemistry as a new paradigm in reaction control
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Spirocyclic dihydropyridines by electrophile-induced dearomatizing cyclization of N-alkenyl pyridinecarboxamides
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Stepwise aromatic nucleophilic substitution in continuous flow. Synthesis of an unsymmetrically substituted 3,5-diamino-benzonitrile library
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Stereocontrolled synthesis of the cis‐hydroxydecalin system: Towards biologically active 19‐nor‐clerodanes
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Stereoselective approaches to 2,3,6-trisubstituted piperidines. An enantiospecific synthesis of quinolizidine (−)-217A
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Stereoselective catalytic synthesis of active pharmaceutical ingredients in homemade 3D‐printed mesoreactors
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Stereoselective metal‐free reduction of chiral imines in batch and flow mode: a convenient strategy for the synthesis of chiral active pharmaceutical ingredients
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Stereoselective reduction of prochiral cyclic 1,3-diketones using different biocatalysts
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Stereoselective syntheses and transformations of chiral 1,3-aminoalcohols and 1,3-diols derived from nopinone
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Stereoselective total synthesis of the marine macrolide sanctolide A
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Straightforward hetero Diels-Alder reactions of nitroso dienophiles by microreactor technology
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Structural assessment of novel spiro-naphthalene-1.2′- [1,3,4]oxadiazol-4-ones prepared under batch and flow chemistry with a concise antifungal and anti(myco)bacterial activity
Saleh, L. Y. et al.; Tetrahedron, 2023, 131, 133231
Structural Effects of Metal Single-Atom Catalysts for Enhanced Photocatalytic Degradation of Gemfibrozil
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Structural identification of petroleum acids by conversion to hydrocarbons and multidimensional gas chromatography-mass spectrometry
Wilde, M. J.; Rowland S. J.; Analytical Chemistry, 2015, 87(16), 8457-8465
Structural requirements for TLR7-selective signaling by 9-(4-piperidinylalkyl)-8-oxoadenine derivatives
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Structural studies of the O-acetyl-containing O-antigen from a Shigella flexneri serotype 6 strain and synthesis of oligosaccharide fragments thereof
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Structurally Diverse Mitochondrial Branched Chain Aminotransferase (BCATm) Leads with Varying Binding Modes Identified by Fragment Screening
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Structure activity relationships of 4-hydroxy-2-pyridones: A novel class of antituberculosis agents
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Structure and reactivity of supported hybrid platinum nanoparticles for the flow hydrogenation of functionalized nitroaromatics
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Structure-based design of potent and ligand-efficient inhibitors of CTX-M class A β-lactamase
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Structure-based optimization of naphthyridones into potent ATAD2 bromodomain inhibitors
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Structure-guided lead optimization of triazolopyrimidine-ring substituents identifies potent plasmodium falciparum dihydroorotate dehydrogenase inhibitors with clinical candidate potential
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Structuring hybrid palladium nanoparticles in metallic monolithic reactors for continuous-flow three-phase alkyne hydrogenation
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Studies of long chain lipids in insects by high temperature gas chromatography and high temperature gas chromatography–mass spectrometry
Sutton, P. A.; Wilde, M. J.; Martin, S. J.; Cvacka, J.; Vrkoslav, V.; Rowland, S. J.; Journal of Chromatography A, 2013, 1297, 236-240
Studies on the continuous-flow synthesis of nonpeptidal bis-tetrahydrofuran moiety of Darunavir
Leao, R. A. C.; Lopes, R. de O.; de M. Bezerra, M. A.; Muniz, M. N.; Casanova, B. B.; Gnoatto, S. C. B.; Gosmann, G.; Kocsis, L.; de Souza, R. O. M. A.; de M. Miranda, L. S.; Journal of Flow Chemistry, 2015, 5(4), 216-219
Studies on the synthesis of the lasubine alkaloids
Aslam, N. F. M.; Simon, O.; Bates, R. W.; Tetrahedron, 2018, 74(38), 5032-5039
Substrate engineering: Effects of different N-protecting groups in the CAL-B-catalysed asymmetric O-acylation of 1-hydroxymethyl-tetrahydro-β-carbolines
Megyesi, R.; Forro, E.; Fulop, F.; Tetrahedron, 2018, 74(21), 2634-2640
Sustainable Drug Discovery of Multi-Target-Directed Ligands for Alzheimer’s Disease
Rossi, M. et al.; J. Med. Chem., 2021, 64(8), 4972-4990
Sydnone Cycloaddition Route to Pyrazole-Based Analogs of Combretastatin A4
Brown, A. W. et al.; J. Med. Chem., 2016, 59, 9473-9488
Synergistic interaction within bifunctional ruthenium nanoparticle/SILP catalysts for the selective hydrodeoxygenation of phenols
Luska, K. L.; Migowski, P.; El Sayed, S.; Leitner, W.; Angew. Chem., 2015, 127(52), 15976-15981
Syntheses of 4-, 5-, 6-, and 7-substituted tryptamine derivatives and the use of a bromine atom as a protecting group
Rene, O.; Fauber, B. P.; Tetrahedron Letters, 2014, 55(4), 830-833
Syntheses of four enantiomers of 2,3-diendo- and 3-endo-aminobicyclo[2.2.2]oct-5-ene-2-exo-carboxylic acid and their saturated analogues
Palko, M.; Hanninen, M. M.; Sillanpaa, R.; Fulop, F.; Molecules, 2013, 18(12), 15080-15093
Synthesis and activity of putative small-molecule inhibitors of the F-Box protein SKP2
Shouksmith, A. E.; Evans, L. E.; Tweddle, D. A.; Miller, D. C.; Willmore, E.; Newell, D. R.; Golding, B. T.; Griffin, R. J.; Aust. J. Chem., 2015, 68(4), 660-679
Synthesis and anticancer activity of a series of norcantharidin analogues
Tarleton, M.; Gilbert, J.; Sakoff, J. A.; McCluskey, A.; Eur. J. Med. Chem., 2012, 54, 573-581
Synthesis and antiviral evaluation of a novel series of homoserine-based inhibitors of the hepatitis C virus NS3/4A serine protease
Alexandre, F-R.; Brandt, G.; Caillet, C.; Chaves, D.; Convard, T.; Derock, M.; Gloux, D.; Griffon, Y.; Lallos, L.; Leroy, F.; Liuzzi, M.; Loi, A-G.; Moulat, L.; Musiu, C.; Parsy, C.; Rahali, H.; Roques, V.; Seifer, M.; Standring, D.; Surleraux, D.; Bioorg. Med. Chem. Lett., 2015, 25(18), 3984-3991
Synthesis and arylation of unprotected sulfonimidamides
Maldonado; M. F.; Sehgelmeble, F.; Bjarnemark, F.; Svensson, M.; Ahman, F.; Arvidsson, P. I.; Tetrahedron, 2012, 68, 7456-7462
Synthesis and biological characterisation of sirtuin inhibitors based on the tenovins
McCarthy, A. R.; Pirrie, L.; Hollick, J. J.; Ronseaux, S.; Campbell, J.; Higgins, M.; Staples, O. D.; Tran, F.; Slawin, A. M. Z.; Lain, S.; Westwood, N. J.; Bioorg. Med. Chem., 2012, 20, 1779-1793
Synthesis and biological evaluation of 1,4-benzodiazepin-2-ones with antitrypanosomal activity
Spencer, J.; Rathnam, R. P.; Harvey, A. L.; Clements, C. J.; Clark, R. L.; Barrett, M. P.; Wong, P. E.; Male, L.; Coles, S. J.; Mackay, S. P.; Bioorg. Med. Chem., 2011, 19, 1802-1815
Synthesis and biological evaluation of 2,3-diarylimidazo[1,2-a]pyridines as antileishmanial agents
Marhadour, S.; Marchand, P.; Pagniez, F.; Bazin, M. A.; Picot, C.; Lozach, O.; Ruchaud, S.; Antoine, M.; Meijer, L.; Rachidi, N.; Le Pape, P.; Eur. J. Med. Chem., 2012, 58, 543-556
Synthesis and biological evaluation of an orally active glycosylated endomorphin-1
Varamini, P.; Mansfeld, F. M.; Blanchfield, J. T.; Wyse, B. D.; Smith, M. T.; Toth, I.; J. Med. Chem., 2012, 55(12), 5859-5867
Synthesis and biological evaluation of dual action cyclo-RGD/SMAC mimetic conjugates targeting αvβ3/αvβ5 integrins and IAP proteins
Mingozzi, M.; Manzoni, L.; Arosio, D.; Dal Corso, A.; Manzotti, M.; Innamorati, F.; Pignataro, L.; Lecis, D.; Delia, D.; Seneci, P.; Gennari, C.; Org. Biomol. Chem., 2014, 12, 3288-3302
Synthesis and biological evaluation of halogenated curcumin analogs as potential nuclear receptor selective agonists
Batie, S.; Lee, J. H.; Jama, R. A:; Browder, D. O.; Montano, L. A.; Huynh, C. C.; Marcus, L. M.; Tsosie, D. G.; Mohammed, Z.; Trang, V.; Marshall, P. A.; Jurutka, P. W.; Wagner, C. E.; Bioorg. Med. Chem., 2013, 21, 693-702
Synthesis and biological evaluation of naphthoquinone analogs as a novel class of proteasome inhibitors
Lawrence, H. R.; Kazi, A.; Luo, Y.; Kendig, R.; Ge, Y.; Jain, S.; Daniel, K.; Santiago, D.; Guida, W. C.; Sebti, S. M.; Bioorg. Med. Chem., 2010, 18(15), 5576-5592
Synthesis and biological evaluation of second-generation tropanol-based androgen receptor modulators
Sunden, H.; Holland, M. C.; Poutiainen, P. K.; Jaaskelainen, T.; Pulkkinen, J. T.; Palvimo, J. J.; Olsson, R.; J. Med. Chem., 2015, 58, 1569-1574
Synthesis and Characterization of Late Transition Metal Complexes of Mono-Acetate Pendant Armed Ethylene Cross-Bridged Tetraazamacrocycles with Promise as Oxidation Catalysts for Dye Bleaching
Hoang, T. et al.; Molecules, 2023, 28(1), 232
Synthesis and cytotoxicity of octahydroepoxyisoindole-7-carboxylic acids and norcantharidin-amide hybrids as norcantharidin analogues
Hizartzidis, L.; Gilbert, J.; Gordon, C. P.; Sakoff, J. A.; McCluskey, A.; ChemMedChem, 2019, 14(12), 1152-1161
Synthesis and photophysical characterization of 1- and 4-(purinyl)triazoles
Redwan, I. N.; Bliman, D.; Tokugawa, M.; Lawson, C.; Grotli, M.; Tetrahedron, 2013, 69(42), 8857-8864
Synthesis and reactivity of 3-amino-1H-pyrazolo[4,3-c]pyridin-4(5H)-ones: development of a novel kinase-focussed library
Smyth, L. A.; Matthews, T. P.; Horton, P. N.; Hursthouse, M. B.; Collins, I.; Tetrahedron, 2010, 66, 2843-2854
Synthesis and solid state study of pyridine- and pyrimidine-based fragment libraries
Spencer, J.; Patel, H.; Callear, S. K.; Coles, S. J.; Deadman, J. J.; Tetrahedron Letters, 2011, 52, 5905-5909
Synthesis and structure-activity relationship studies of 2,4-thiazolidinediones and analogous heterocycles as inhibitors of dihydrodipicolinate synthase
Christoff, R. M. et al.; Bioorg. Med. Chem., 2021, 52, 116518
Synthesis and structure–activity relationship studies of 4-((2-hydroxy-3-methoxybenzyl)amino)benzenesulfonamide derivatives as potent and selective inhibitors of 12-lipoxygenase
Luci, D. K.; Jameson, J. B.; Yasgar, A.; Diaz, G.; Joshi, N.; Kantz, A.; Markham, K., Perry, S.; Kuhn, N.; Yeung, J., Kerns, E. H.; Schultz, L.; Holinstat, M.; Nadler, J. L.; Taylor-Fishwick, D. A.; Jadhav, A.; Simeonov, A.; Holman, T. R.; Maloney, D. J.; J. Med. Chem., 2014, 57(2), 495-506
Synthesis and structure-activity relationship studies of N-benzyl-2-phenylpyrimidin-4-amine derivatives as potent USP1/UAF1 deubiquitinase inhibitors with anticancer activity against nonsmall cell lung cancer
Dexheimer, T. S.; Rosenthal, A. S.; Luci, D. K.; Liang, Q.; Villamil, M. A.; Chen, J.; Sun, H.; Kerns, E. H.; Simeonov, A.; Jadhav, a.; Zhuang, Z.; Maloney, D. J.; J. Med. Chem., 2014, 57(19), 8099-8110
Synthesis and structure–activity relationships of N‐(4‐benzamidino)‐oxazolidinones–potent and selective inhibitors of kallikrein‐related peptidase 6
De Vita, E.; Smits, N.; van den Hurk, H.; Beck, E. M.; Hewitt, J.; Baillie, G.; Russell, E.; Pannifer, A.; Hamon, V.; Morrison, A.; McElroy, S. P.; Jones, P.; Ignatenko, N.; Gunkel, N.; Miller, A. K.; ChemMedChem, 2019, accepted manuscript
Synthesis and structure–activity relationship (SAR) of 2-methyl-4-oxo-3-oxetanylcarbamic acid esters, a class of potent N-acylethanolamine acid amidase (NAAA) inhibitors
Ponzano, S.; Bertozzi, F.; Mengatto, L.; Dionisi, M.; Armirotti, A.; Romeo, E.; Berteotti, A.; Fiorelli, C.; Tarozzo, G.; Reggiani, A.; Duranti, A.; Tarzia, G.; Mor, M.; Cavalli, A.; Piomelli, D.; Bandiera, T.; J. Med. Chem., 2013, 56(17), 6917-6934
Synthesis, anti‐tubulin and antiproliferative SAR of steroidomimetic dihydroisoquinolinones
Leese, M. P.; Jourdan, F. L.; Major, M. R.; Dohle, W.; Thomas, M. P.; Hamel, E.; Ferrandis, E.; Mahon, M. F.; Newman, S. P.; Purohit, A.; Potter, B. V. L.; ChemMedChem, 2014, 9, 798-812
Synthesis, antitubulin, and antiproliferative SAR of C3/C1‐substituted tetrahydroisoquinolines
Dohle, W.; Leese, M. P.; Jourdan, F. L.; Major, M. R.; Bai, R.; Hamel, E.; Ferrandis, E.; Kasprzyk, P. G.; Fiore, A.; Newman, S. P.; Purohit, A.; Potter, B. V. L.; ChemMedChem, 2014, 9, 350-370
Synthesis, biological evaluation, and molecular modeling of new 3‑(cyclopentyloxy)-4-methoxybenzaldehyde O‑(2-(2,6-dimethylmorpholino)-2-oxoethyl) oxime (GEBR-7b) related phosphodiesterase 4D (PDE4D) inhibitors
Brullo, C.; Massa, M.; Rocca, M; Rotolo, C.; Guariento, S.; Rivera, D.; Ricciarelli, R.; Fedele, E.; Fossa, P.; Bruno, O.; J. Med. Chem., 2014, 57(16), 7061-7072
Synthesis, biological evaluation, and utility of fluorescent ligands targeting the μ-opioid receptor
Schembri, L. S.; Stoddart, L. A.; Briddon, S. J.; Kellam, B.; Canals, M.; Graham, B.; Scammells, P. J.; J. Med. Chem., 2015, 58(24), 9754-9767
Synthesis, evaluation, and radiolabeling of new potent positive allosteric modulators of the metabotropic glutamate receptor 2 as potential tracers for positron emission tomography imaging
Andres, J. I.; Alcazar, J.; Cid, J. M.; De Angelis, M., Iturrino, L.; Langlois, X.; Lavreysen, H.; Trabanco, A. A.; Celen, S.; Bormans, G.; J. Med. Chem., 2012, 55, 8685-8699
Synthesis, in vivo occupancy, and radiolabeling of potent phosphodiesterase subtype-10 inhibitors as candidates for positron emission tomography imaging
Andres, J-I.; De Angelis, M.; Alcazar, J.; Iturrino, L.; Langlois, X.; Dedeurwaerdere, S.; Lenaerts, I.; Vanhoof, G.; Celen, S.; Bormans, G.; J. Med. Chem., 2011, 54, 5820-5835
Synthesis of 12β-Methyl-18-nor-bile Acids
Luxenburger, A. et al.; ACS Omega, 2021, 6(38), 25019-25039
Synthesis of 2,6-Dimethyltyrosine-Like Amino Acids through Pinacolinamide-Enabled C-H Dimethylation of 4-Dibenzylamino Phenylalanine
Illuminati, D. et al.; J. Org. Chem., 2022, 87, 5, 2580-2589
Synthesis of 3-arylated 3,4-dihydrocoumarins: Combining continuous flow hydrogenation with laccase-catalysed oxidation
Suljic, S.; Pietruszka, J.; Adv. Synth. Catal., 2014, 356(5), 1007-1020
Synthesis of 3-nitropyrrolidines via dipolar cycloaddition reactions using a modular flow reactor
Baumann, M.; Baxendale, I. R.; Ley, S. V.; Synlett, 2010, 5, 749-752
Synthesis of 3‐Hydroxypipecolic Acids
Cochi, A.; Pardo, D. G.; Cossy, J.; Eur. J. Org. Chem., 2013, 2013(5), 809-829
Synthesis of 4-fluoromethylsydnones and their participation in alkyne cycloaddition reactions
Foster, R. S.; Adams, H.; Jakobi, H.; Harrity, J. P. A.; J. Org. Chem., 2013, 78(8), 4049-4064
Synthesis of 5‐bromomethylfurfural from cellulose as a potential intermediate for biofuel
Kumari, N.; Olesen, J. K.; Pedersen, C. M.; Bols, M.; Eur. J. Org. Chem., 2011, 2011(7), 1266-1270
Synthesis of a biphenyl library for studies of hydrogen bonding in the solid state
Baltus, C. B.; Press, N. J.; Antonijevic, M. D.; Tizzard, G. J.; Coles, S. J.; Spencer, J.; Tetrahedron, 2012, 68(45), 9272-9277
Synthesis of a drug-like focused library of trisubstituted pyrrolidines using integrated flow chemistry and batch methods
Baumann, M.; Baxendale, I. R.; Kuratli, C.; Ley, S. V.; Martin, R. E.; Schneider, J.; ACS Comb. Sci., 2011, 13(4), 405-413
Synthesis of a new family of acyclic nucleoside phosphonates, analogues of TPases transition states
Dayde, B.; Benzaria, S.; Pierra, C.; Gosselin, G.; Surleraux, D.; Volle, J.; Pirat, J.; Virieux, D.; Org. Biomol. Chem, 2012, 10, 3448-3454
Synthesis of a novel C2/C2′-aryl-substituted pyrrolo[2,1-c][1,4]benzodiazepine dimer prodrug with improved water solubility and reduced DNA reaction rate
Howard, P. W.; Chen, Z.; Gregson, S. J.; Masterson, L. A.; Tiberghien, A. C.; Cooper, N.; Fang, M.; Coffils, M. J.; Klee, S.; Hartley, J. A.; Thurston, D. E.; Bioorg. Med. Chem. Lett. 2009, 19(22), 6463-6466
Synthesis of a (piperazin-1-ylmethyl)biaryl library via microwave-mediated Suzuki–Miyaura cross-couplings
Spencer, J.; Baltus, C. B.; Press, N. J.; Harrington, R. W.; Clegg, W.; Tetrahedron Letters, 2011, 52(31), 3963-3968
Synthesis of a Streptococcus pyogenes vaccine candidate based on the M protein PL1 epitope
Simerska, P.; Lu, H.; Toth, I.; Bioorg. Med. Chem. Lett., 2009, 19(3), 821-824
Synthesis of a tetrasaccharide related to the triterpenoid saponin Bellisoside isolated from Bellis perennis (compositae)
Mandal, S.; Sharma, N.; Mukhopadhyay, B.; Tetrahedron: Asymmetry, 2010, 21, 2172-2176
Synthesis of amines from alcohols in a nonepimerizing one-pot sequence – Synthesis of bioactive compounds: Cinacalcet and dexoxadrol
Guerin, C.; Bellosta, V.; Guillamot, G.; Cossy, J.; Eur. J. Org. Chem., 2012, 15, 2990-3000
Synthesis of an azabicyclic framework towards (±)-actinophyllic acid
Mortimer, D.; Whiting, M.; Harrity, J. P. A.; Jones, S.; Coldham, I.; Tetrahedron Letters, 2014, 55, 1255-1257
Synthesis of an undecasaccharide featuring an oligomannosidic heptasaccharide and a bacterial Kdo-lipid A backbone for eliciting neutralizing antibodies to mammalian oligomannose on the HIV-1 envelope spike
Trattnig, N.; Blaukopf, M.; Bruxelle, J-F.; Pantophlet, R.; Kosma, P.; JACS, 2019, 141(19), 7946-7954
Synthesis of aromatic 13C/2H-α-ketoacid precursors to be used in selective phenylalanine and tyrosine protein labelling
Lichtenecker, R. J.; Org. Biomol. Chem., 2014, 12, 7551-7560
Synthesis of benzannulated spiroketals using an oxidative radical cyclization
Sperry, J.; Liu, Y-C.; Wilson, Z. E.; Hubert, J. G.; Brimble, M. A.; Synthesis, 2011, 9, 1383-1398
Synthesis of bioderived cinnolines and their flow-based conversion into 1,4-dihydrocinnoline derivatives
Devlin, J.; Clogher, R.; Baumann, M.; Synlett, 2019, accepted manuscript
Synthesis of bivalent lactosides based on terephthalamide, N,N-diglucosylterephthalamide, and glycophane scaffolds and assessment of their inhibitory capacity on medically relevant lectins
Leyden, R.; Velasco-Torrijos, T.; Andre, S.; Gouin, S.; Gabius, H-J.; Murphy, P. V.; J. Org. Chem., 2009, 74(23), 9010-9026
Synthesis of Chalcones Derivatives and Their Biological Activities: A Review
Elkanzi, N. A. A. et al.; ACS Omega, 2022, 7, 27769-27786
Synthesis of condensed heterocycles by the Gould-Jacobs reaction in a novel three-mode pyrolysis reactor
Lengyel, L. C.; Sipos, G.; Sipocz, T.; Vago, T.; Dorman, G.; Gerencser, J.; Makara, G.; Darvas, F.; Org. Process Res. Dev., 2015, 19(3), 399-409
Synthesis of cross‐linked glycopeptides and ureas by a mechanochemical, solvent‐free reaction and determination of their structural properties by TEM and X‐ray crystallography
Kumar, V.; Giri, S. K.; Venugopalan, P.; Kartha, K. P. R.; ChemPlusChem, 2014, 79(11), 1605-1613
Synthesis of four (4″-, 2″-, 2′-, and 6-) monodeoxy analogs of the trisaccharide α-d-Glcp-(1→3)-α-d-Manp-(1→2)-α-d-ManpOMe recognized by Calreticulin/Calnexin
Glinschert, A.; Oscarson, S.; Carbohydrate Research, 2015, 414, 65-71
Synthesis of functionalized 3-hydroxypiperidines
Wijdeven, M. A.; van Delft, F. L.; Rutjes, F. P. J. T.; Tetrahedron, 2010, 66, 5623-5636
Synthesis of Fused Pyrimidinone and Quinolone Derivatives in an Automated High Temperature and High Pressure Flow Reactor
Tsoung, J. et al.; J. Org. Chem., 2017, 82, 1073-1084
Synthesis of Highly Functionalized 4-Aminoquinolines
Wezeman, T. et al.; Angew. Chem. Int. Ed., 2016, 55, 3823-3827
Synthesis of highly substituted nitropyrrolidines, nitropyrrolizines and nitropyrroles via multicomponent-multistep sequences within a flow reactor
Baumann, M.; Baxendale, I. R.; Kirschning, A.; Ley, S. V.; Wegner, J.; Heterocycles, 2011, 82(2), 1297-1316
Synthesis of hydroxylated pyrrolidines by allenic cyclisation
Ng, P. S. et al.; Tetrahedron, 2016, 72, 6356-6362
Synthesis of α-substituted vinylsulfonium salts and their application as annulation reagents in the formation of epoxide- and cyclopropane-fused heterocycles
Matlock, J. V.; Fritz, S. P.; Harrison, S. A.; Coe, D. M.; McGarrigle, E. M.; Aggarwal, V. K.; J. Org. Chem., 2014, 79, 10226-10239
Synthesis of L-[5-11C]Leucine and L-α-[5-11C]Methylleucine via Pd0-mediated 11C-Methylation and Microfluidic Hydrogenation: Potentiality of Leucine PET Probes for Tumor Imaging
Takatani, S. et al.; ChemMedChem, 2021, 16(21), 3271-3279
Synthesis of laminarin fragments and evaluation of a β-(1,3) glucan hexasaccaride-CRM197 conjugate as vaccine candidate against Candida albicans
Adamo, R.; Tontini, M.; Brogioni, G.; Romano, M. R.; Contantini, G.; Danieli, E.; Proietti, D.; Berti, F.; Constantino, P.; Journal of Carbohydrate Chemistry, 2011, 30, 249-280
Synthesis of macrolide-saccharide hybrids by ring-closing metathesis of precursors derived from glycitols and benzoic acids
Matos, M-C.; Murphy, P. V.; J. Org. Chem., 2007, 72, 1803-1806
Synthesis of Mepivacaine and Its Analogues by a Continuous-Flow Tandem Hydrogenation/Reductive Amination Strategy
Suveges, N. S. et al.; Eur. J. Org. Chem., 2017, 6511-6517
Synthesis of N-aryl spiro-sulfamides as potential glycogen phosphorylase inhibitors
Tite, T.; Tomas, L.; Docsa, T.; Gergely, P.; Kovensky, J.; Gueyrard, D.; Wadouachi, A.; Tetrahedron Letters, 2012, 53, 959-961
Synthesis of N-hydroxypyrazin-2(1H)-ones via selective O-debenzylation of 1-benzyloxypyrazin-2(1H)-ones using flow methodology
Mai, A. H.; De Borggraeve, W. M.; J. Flow Chem., 2015, 5(1), 6-10
Synthesis of N-propynyl analogues of peptide nucleic acid (PNA) monomers and their use in the click reaction to prepare N-functionalized PNAs
Howarth, N. M.; Ricci, J.; Tetrahedron, 2011, 67, 9588-9594
Synthesis of natural and unnatural cyclooligomeric depsipeptides enabled by flow chemistry
Lucke, D.; Dalton, T.; Ley, S. V.; Wilson Z. E.; Chem. Eur. J., 2016, 22(12), 4206-4217
Synthesis of new 18F-radiolabeled silicon-based nitroimidazole compounds
Joyard, Y.; Azzouz, R.; Bischoff, L.; Papamicael, C.; Labar, D.; Bol, A.; Bol, V.; Vera, P.; Gregoire, V.; Levacher, V.; Bohn, P.; Bioorg. Med. Chem., 2013, 21, 3680-3688
Synthesis of new oxathiazinane dioxides and their in vitro cancer cell growth inhibitory activity
Borcard, F.; Baud, M.; Bello, C.; Dal Bello, G.; Grossi, F.; Pronzato, P.; Cea, M.; Nencioni, A.; Vogel, P.; Bioorg. Med. Chem. Lett., 2010, 20(17), 5353-5356
Synthesis of Novel Camphor-Derived Bifunctional Thiourea Organocatalysts
Ricko, S.; Golobic, A.; Svete, J.; Stanovnik, B.; Groselj, U.; Chirality, 2015, 27(1), 39-52
Synthesis of novel Iron(III) chelators based on triaza macrocycle backbone and 1-hydroxy-2(H)-pyridin-2-one coordinating groups and their evaluation as antimicrobial agents
Workman, D. G.; Hunter, M.; Dover, L. G.; Tetard, D.; Journal of Inorganic Biochemistry, 2016, 160, 49-58
Synthesis of oxaspiropiperidines as a strategy for lowering logD
Cernak, T.; Dykstra, K.; Levorse, D.; Verras, A.; Balkovec, J.; Nargund, R.; DeVita, R.; Tetrahedron Letters, 2011, 52, 6457-6459
Synthesis of phenols via fluoride-free oxidation of arylsilanes and arylmethoxysilanes
Rayment, E. J.; Summerhill, N.; Anderson, E. A.; J. Org. Chem., 2012, 77(16), 7052-7060
Synthesis of riboflavines, quinoxalinones and benzodiazepines through chemoselective flow based hydrogenations
Baumann, M.; Baxendale, I. R.; Hornung, C. H.; Ley, S. V.; Rojo, M. V; Roper, K. A.; Molecules, 2014, 19(7), 9736-9759
Synthesis of spirocyclic thiazolidinediones using ring-closing metathesis and one-pot sequential ring-closing/cross metathesis
Dhara, K.; Paladhi, S.; Midya, G. C.; Dash, J.; Org. Biomol. Chem., 2011, 9, 3801-3807
Synthesis of Staphylococcus aureus type 5 capsular polysaccharide repeating unit using novel L-FucNAc and D-FucNAc synthons and immunochemical evaluation
Danieli, E.; Proietti, D.; Brogioni, G.; Romano, M. R.; Cappelletti, E.; Tontini, M.; Berti, F.; Lay, L.; Costantino, P.; Adamo, R.; Bioorg. Med. Chem., 2012, 20, 6403-6415
Synthesis of sugar-lactams from azides of glucuronic acid
Loukou, C.; Tosin, M.; Muller-Bunz, H.; Murphy, P. V.; Carbohydrate Research, 2007, 342(12-13), 1953-1959
Synthesis of symmetric dinitro‐functionalised Tröger’s base analogues
Bhuiyan, M. D. H.; Mahon, A. B.; Jensen, P.; Clegg, J. K.; Try, A. C.; Eur. J. Org. Chem., 2009, 5, 687-698
Synthesis of 2,6,8,12-tetraacetyl-2,4,6,8,10,12-hexaazaisowurtzitane (TAIW) from 2,6,8,12-tetraacetyl-4,10-dibenzyl-2,4,6,8,10,12-hexaazaisowurtzitane (TADBIW) by catalytic hydrogenolysis using a continuous flow process
Dong, K.; Sun, C. H.; Song, J. W., Wei, G. X.; Pang, S. P.; Org. Process Res. Dev., 2014, 18, 1321-1325
Synthesis of tetrazole analogues of amino acids using Fmoc chemistry: isolation of amino free tetrazoles and their incorporation into peptides
Sureshbabu, V. V.; Venkataramanarao, R.; Naik, S. A.; Chennakirshnareddy, G.; Tetrahedron Letters, 2007, 48(39), 7038-7041
Synthesis of the tetrasaccharide related to the repeating unit of the O-antigen from Azospirillum brasilense Jm125A2 in the form of its 2-aminoethyl glycoside
Sarkar, V. et al.; Carbohydrate Research, 2018, 470, 13-18
Synthesis of the tetrasaccharide repeating unit of the β-Kdo-containing exopolysaccharide from Burkholderia pseudomallei and B. cepacia complex
Laroussarie, A.; Barycza, B.; Andriamboavonjy, H.; Kenfack, M. T.; Bleriot, Y.; Gauthier, C.; J. Org. Chem., 2015, 80(20), 10386-10396
Synthesis of the tetrasaccharide repeating unit of the O-antigen from Pseudomonas putida BIM B-1100 having rare D-Quip3NAc
Bera, M. et al.; Carbohydrate Research, 2020, 489, 107955
Synthesis of the tetrasaccharide repeating unit of the O-glycan from the polar flagellum flagellin of Azospirillum brasilense Sp7
Pal, K. B.; Mukhopadhyay, B.; Carbohydrate Research, 2014, 400, 9-13
Synthesis of the trisaccharide repeating unit of the lipopolysaccharide from Moritella viscosa strain M2-226
Pal, K. B.; Verma, P. R.; Gupta, T.; Mukhopadhyay, B.; Journal of Carbohydrate Chemistry, 2015, 34(4), 173-182
Synthesis of two trisaccharides related to the hepatoprotective phenylethanoids leonoside E and F isolated from Leonurus japonicus Houtt
Budhadev, D.; Mukhopadhyay, B.; Carbohydrate Research, 2014, 384, 51-55
Synthesis of unique scaffolds via Diels-Alder cycloadditions of tetrasubstituated cyclohexadienes
Jones, A. L.; Snyder, J. K.; Organic Letters, 2010, 12(7), 1592-1595
Synthesis of unsaturated secondary amines by direct reductive amination of aliphatic aldehydes with nitroarenes over Au/Al2O3 catalyst in continuous flow mode
Artiukha, E. A. et al.; RSC Adv., 2016, 6, 88366-88372
Synthesis of γ-valerolactone using a continuous-flow reactor
Tukacs, J. M.; Jones, R. V.; Darvas, F.; Dibo, G.; Lezsak, G.; Mika, L. T.; RSC Adv., 2013, 3, 16283-16287
Synthesis, Properties, and Two-Dimensional Adsorption Characteristics of [6]Hexahelicene-7-carboxylic acid
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