Publications
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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.
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Browse the list of all published scientific papers, last update: 2023/10/17
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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. et al; J. Med. Chem., 2019, 62(23), 10848-10866
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
4b,5,6,9-Tetrahydro-7H-dibenzo[c,e]pyrrolo[1,2-a]azepin-7-one
Boichenko, M. A. et al.; Molbank, 2019, 2019, M1061
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 High‐Throughput Composite Catalyst based on Nickel Carbon Cubes for the Hydrogenation of 5‐Hydroxymethylfurfural to 2,5‐Dimethylfuran
Mani, C. M. et al.; ChemCatChem, 2017, 9, 3388-3394
A Meldrum’s Acid Based Multicomponent Synthesis of N-Fmoc isoxazolidin-5-ones: Entry to N-Fmoc-β-amino Acids
Le Foll Devaux, A. et al.; Eur. J. Org. Chem., 2017, 3265-3273
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, low footprint and scalable flow platform for the expedient α-aminohydroxylation of enolizable ketones
Kassin, V-E. H. et al.; Green Chemistry, 2021, 23, 2336-2351
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 novel nano-palladium catalyst for continuous-flow chemoselective hydrogenation reactions
Goszewska, I. et al.; Catalysis Communications, 2017, 94, 65-68
A Novel One-pot Benzimidazole Ring Formation via a Continuous Flow Selective Reductive Cyclization Method
Szabo, B. et al.; Curr. Org. Chem., 2018, 22(19), 1940-1944
A novel pathway for the thermolysis of N-nitrosoanthranilates using flash vacuum pyrolysis leading to 7-aminophthalides
Zlatkovic, D. et al.; Org. Biomol. Chem., 2020, 18, 8371-8375
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 compact flow platform for the neutralization of a mustard gas simulant with air and light
Emmanuel, N. et al.; Green Chemistry, 2020, 22, 4105-4115
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 step forward towards sustainable aerobic alcohol oxidation: new and revised catalysts based on transition metals on solid supports
Parmeggiani, C. et al.; Green Chemistry, 2017, 19, 2030-2050
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 streamlined synthesis of the neurosteroid 3β-methoxypregnenolone assisted by a statistical experimental design and automation
Mancino, V. et al.; React. Chem. Eng., 2020, 5, 300-307
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
Accelerating Biocatalytic Hydrogenations using the H-Cube Flow Reactor
Poznansky, B. et al.; Catalysis, 2020, Working paper
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 In-Line Purification Technologies in Multistep Continuous Flow Pharmaceutical Synthesis
Lei, Z. et al.; Org. Process Res. Dev., 2023, Accepted manuscript
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
Ag–In–Zn–S Quaternary Nanocrystals Prepared from InCl2 Precursor: Photophysical and Spectroscopic Properties and Application as Visible Light Photocatalysts of Aromatic Aldehyde Photoreduction
Kowalik, P. et al.; Chem. Mater., 2023, Accepted manuscript
Aiming to Miss a Moving Target: Bromo and Extra Terminal Domain (BET) Selectivity in Constrained ATAD2 Inhibitors
Bamborough, P. et al.; J. Med. Chem., 2018, 18, 8321-8336
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
Ambient Processed rGO/Ti3CNTx MXene Thin Film with High Oxidation Stability, Photosensitivity, and Self-Cleaning Potential
Purbayanto, M. A. K. et al.; ACS Appl. Nano Mater., 2023, Accepted manuscript
Amino-Modified Silica-Supported Copper-Palladium Alloy. Synthesis and Use in Selective Hydrogenation of Disubstituted Nitroarenes in a Flow Micro Reactor
Nurmukhametova, A. T. et al.; Russian J. Org. Chem., 2019, 55, 1-6
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 Enantioselective Approach to Pinguisane Sesquiterpenes: Total Synthesis of (–)-Pinguisenol and (–)-Isonaviculol
Singh, S. et al.; Eur. J. Org. Chem., 2017, 2824-2830
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 effective synthesis of polynuclear tetraamines, monomers for polyheteroarylenes
Begunov, R. S. et al.; Russian Chemical Bulletin, 2018, 67, 1072-1077
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 Intramolecular Diels–Alder Furan (IMDAF) Approach towards the Synthesis of Isoindolo[2,1-a]quinazolines and Isoindolo-[1,2-b]quinazolines
Revutskaya E. L. et al.; Synthesis, 2017, 49(16), 3749-3767
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
Anthranilic acid, the new player in the ensemble of aromatic residue labeling precursor compounds
Schorghuber, J. et al.; J. Biomol. NMR, 2017, 69, 13-22
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
Application of reactor engineering concepts in continuous flow chemistry: a review
Neyt, N. C. et al.; React. Chem. Eng., 2021, 6, 1295-1326
Applying flow chemistry: Methods, materials, and multistep synthesis
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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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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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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 and Reactions of Pyrroline, Piperidine Nitroxide Phosphonates
Isbera, M. et al.; Molecules, 2020, 25, 2430
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 Antimicrobial Studies of New Spiropyran Quinazolinone Derivatives with Amide, Urea, and Sulfonamide Moieties
Poojari, S. et al.; J. Heterocyclic Chem., 2017, 54(6), 3527-3537
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 pharmacological activity of the epimers of hexahydrocannabinol (HHC)
Russo, F. et al.; Sci. Rep., 2023, 13, 11061
Synthesis and Pharmacological Characterization of Conformationally Restricted Retigabine Analogues as Novel Neuronal Kv7 Channel Activators
Ostacolo, C. et al.; J. Med. Chem., 2020, 63(1), 163-185
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 reactivity of new amide-substituted oxindole derivatives
Ignatov, A. A. et al.; Tetrahedron, 2017, 73, 6887-6893
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 Structural Elucidation of 1,2-Disubstituted 3-Fluoropiperidines
Fischer, P. et al.; Eur. J. Org. Chem., 2020, 2020(9), 1165-1176
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, Mesomorphism and the Optical Properties of Alkyl-Deuterated Nematogenic 4-[(2,6-Difluorophenyl)ethynyl]biphenyls
Herman, J. et al.; Materials, 2021, 14, 4653
Synthesis of 12β-Methyl-18-nor-bile Acids
Luxenburger, A. et al.; ACS Omega, 2021, 6(38), 25019-25039
Synthesis of 1,5-Anhydro-D-glycero-D-gluco-heptitol Derivatives as Potential Inhibitors of Bacterial Heptose Biosynthetic Pathways
Blaukopf, M. et al.; Synthesis, 2017, 49(24), 5320-5334
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 Nitroxide Spin-labeled Varenicline (Chantix) Derivative
Bognar, B. et al.; Org. Prep. and Proc. Int., 2021, 53(3), 311-315
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 Pentasaccharide Fragment Related to the Inner Core Region of Rhizobial and Agrobacterial Lipopolysaccharides
Trattnig, N. et al.; J. Org. Chem., 2017, 82, 12346-12358
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 Galactoacrylamide and Study of Stimuli-Responsive Fluorescent Hierarchical Self-Assembly-Promoted Specific Interactions with Proteins
Ajish, J. K. et al.; ChemistrySelect, 2023, 8(37), e202301497
Synthesis of Highly Functionalized 4-Aminoquinolines
Wezeman, T. et al.; Angew. Chem. Int. Ed., 2016, 55, 3823-3827
Synthesis of Highly Reactive Ketenimines via Photochemical Rearrangement of Isoxazoles
Bracken, C. et al.; Org. Lett., 2023, Accepted manuscript
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 new tetrahydropyridopyrazine derivatives via continuous flow chemistry approach and their spectroscopic characterizations
Parmar, N. D. et al.; J. Heterocyclic Chem., 2021, 58(7), 1437-1445
Synthesis of Nontoxic Protoflavone Derivatives through Selective Continuous‐Flow Hydrogenation of the Flavonoid B‐Ring
Otvos, S. B. et al.; ChemPlusChem, 2018, 83(2), 72-76
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 Polyanionic C5-Modified 2′-Deoxyuridine and 2′-Deoxycytidine-5′-Triphosphates and Their Properties as Substrates for DNA Polymerases
Dutson, C. et al.; Molecules, 2021, 26, 2250
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 secondary amines by reductive amination of aldehydes with nitroarenes over supported copper catalysts in a flow reactor
Artiukha, E. A. et al.; Catalysis Communications, 2017, 102, 108-113
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 Hexasaccharide Related to the Exopolysaccharide from Lactobacillus mucosae VG1 through Regioselective Glycosylation
Adak, A. et al.; Org. Lett., 2023, 25(25), 4711–4714
Synthesis of the Lipophilic Amine Tail of Abediterol Enabled by Multiphase Flow Transformations
Garcia-Lacuna, J. et al.; Org. Process Res. Dev., 2021, 25, 947-959
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
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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
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Synthesis of the trisaccharide repeating unit of the lipopolysaccharide from Moritella viscosa strain M2-226
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Synthesis of two trisaccharides related to the hepatoprotective phenylethanoids leonoside E and F isolated from Leonurus japonicus Houtt
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Synthesis of unique scaffolds via Diels-Alder cycloadditions of tetrasubstituated cyclohexadienes
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Synthesis of unsaturated secondary amines by direct reductive amination of aliphatic aldehydes with nitroarenes over Au/Al2O3 catalyst in continuous flow mode
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Synthesis of γ-valerolactone using a continuous-flow reactor
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Synthesis, Properties, and Two-Dimensional Adsorption Characteristics of [6]Hexahelicene-7-carboxylic acid
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Synthesis, SAR, and pharmacological characterization of brain penetrant P2X7 receptor antagonists
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Synthesis, structure–activity, and structure–stability relationships of 2‐substituted‐N‐(4‐oxo‐3‐oxetanyl) N‐acylethanolamine acid amidase (NAAA) inhibitors
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Synthetic Access to Noncanonical Strigolactones: Syntheses of Carlactonic Acid and Methyl Carlactonoate
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Synthetic approaches to the C11–C27 fragments of bryostatins
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Synthetic studies toward the C32–C46 segment of hemicalide. Assignment of the relative configuration of the C36–C42 subunit
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Systematic evaluation of the palladium-catalyzed hydrogenation under flow conditions
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Tacrine-resveratrol fused hybrids as multi-target-directed ligands against Alzheimer’s disease
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Tailoring nitrogen-doped carbons as hosts for single-atom catalysts
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Targeting Cytotoxic Agents through EGFR-Mediated Covalent Binding and Release
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Technological Innovations in Photochemistry for Organic Synthesis: Flow Chemistry, High-Throughput Experimentation, Scale-up, and Photoelectrochemistry
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Telescoped synthesis of vicinal diamines via ring-opening of electrochemically generated aziridines in flow
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The assembly of integrated continuous flow platform for on-demand rosiglitazone and pioglitazone synthesis
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The continuous synthesis and application of graphene supported palladium nanoparticles: a highly effective catalyst for Suzuki-Miyaura cross-coupling reactions
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The Cooperative Research Centre for Cancer Therapeutics: bridging the gap between leading cancer research at Australia’s universities and developing novel cancer drugs
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The Current Role of Microfluidics in Radiofluorination Chemistry
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The first case of competitive heterogeneously catalyzed hydrogenation using continuous-flow fixed-bed reactor system: Hydrogenation of binary mixtures of activated ketones on Pt-alumina and on Pt-alumina-cinchonidine catalysts
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The integration of flow reactors into synthetic organic chemistry
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The renascence of continuous-flow peptide synthesis – an abridged account of solid and solution-based approaches
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Thermochemiluminescence-Based Sensitive Probes: Synthesis and Photophysical Characterization of Acridine-Containing 1,2-Dioxetanes Focusing on Fluorophore Push-Pull Effects
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Jensen, K. F.; Reizman, B. J.; Newman, S. G.; Lab. Chip, 2014, 14, 3206-3212
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Topographical mapping of isoform-selectivity determinants for J-channel-binding inhibitors of sphingosine kinases 1 and 2
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Total chemical synthesis of PSMA-11: API for 68Ga-PSMA-11 used for prostate cancer diagnosis
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Total synthesis and biological evaluation of tubulysin analogues
Colombo, R.; Wang, Z.; Han, J.; Balachandran, R.; Daghestani, H. N.; Camarco, D. P.; Vogt, A.; Day, B. W.; Mendel, D.; Wipf, P.; J. Org. Chem., 2016, 81(21), 10302-10320
Total synthesis of (±)-monomorine
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Total synthesis of (±)-taiwaniaquinol F and related taiwaniaquinoids
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Total synthesis of aignopsanes, a class of sesquiterpenes: (+)‐Aignopsanoic acid A, (−)‐methyl aignopsanoate A, and (−)‐isoaignopsanoic A
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Total Synthesis of GE81112A: An Orthoester-Based Approach
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Total Synthesis of Marine-Derived Azole Resistant Antifungal Agent (–)-Melearoride A and Antibiotic (–)-PF1163B
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Total synthesis of the isoquinolinium metabolite ETM‑204 of Trabectidin
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Toward a continuous-flow synthesis of Boscalid®
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Toward the synthesis of noroxymorphone via aerobic palladium-catalyzed continuous flow N-demethylation strategies
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Itabaiana, I., Jr.; Soter de Mariz e Miranda, L.; de Souza, R. O. M. A.; Journal of Molecular Catalysis B: Enzymatic, 2013, 85-86, 1-9
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Towards sustainable hydrogenation of 5-(hydroxymethyl)furfural: a two-stage continuous process in aqueous media over RANEY® catalysts
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Towards the development of chromone-based MEK1/2 modulators
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Transfer hydrogenation of levulinic acid under hydrothermal conditions catalyzed by sulfate as a temperature-switchable base
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Translating high-temperature microwave chemistry to scalable continuous flow processes
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Treatments of lignocellulosic hydrolysates and continuous-flow hydrogenation of xylose to xylitol
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Triflic Acid-Catalyzed Synthesis of Indole-Substituted Indane Derivatives via In Situ Formed Acetal-Facilitated Nucleophilic Addition and 4π-Electron-5-Carbon Electrocyclization Sequence
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Trisubstituted thiazoles as potent and selective inhibitors of Plasmodium falciparum protein kinase G (PfPKG)
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Tunability and scalability of single-atom catalysts based on carbon nitride
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Turbostratic carbon supported palladium as an efficient catalyst for reductive purification of water from trichloroethylene
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Two-photon fluorescent chemosensors based on the GFP-chromophore for the detection of Zn2+ in biological samples – From design to application
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Two step continuous-flow synthesis of benzocaine
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Two-Step One-Pot Reductive Amination of Furanic Aldehydes Using CuAlOx Catalyst in a Flow Reactor
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Using chemical probes to investigate the sub-inhibitory effects of azithromycin
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Using continuous processes to increase production
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USP7 small-molecule inhibitors interfere with ubiquitin binding
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Visually following the hydrogenation of curcumin to tetrahydrocurcumin in a natural product experiment that enhances student understanding of NMR spectroscopy
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VUT-MK142: a new cardiomyogenic small molecule promoting the differentiation of pre-cardiac mesoderm into cardiomyocytes
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Wet-Chemical Etching and Delamination of MoAlB into MBene and Its Outstanding Photocatalytic Performance
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Yolk‐shell‐mesostructured silica‐supported dual molecular catalyst for enantioselective tandem reactions
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