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Photoredox‐Catalyzed Preparation of Sulfones Using Bis‐Piperidine Sulfur Dioxide – An Underutilized Reagent for SO<sub>2</sub> Transfer.
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- Chemistry - A European Journal, 2024, v. 30, n. 12, p. 1, doi. 10.1002/chem.202303976
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The Evolution of Flow Chemistry: An Opinion on Factors Driving Innovation.
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- Chimia, 2023, v. 77, n. 5, p. 288, doi. 10.2533/chimia.2023.288
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A Practical Method for Continuous Production of sp3‐Rich Compounds from (Hetero)Aryl Halides and Redox‐Active Esters.
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- Chemistry - A European Journal, 2020, v. 26, n. 1, p. 186, doi. 10.1002/chem.201905048
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Direct Oxidation of Csp<sup>3</sup>−H bonds using in Situ Generated Trifluoromethylated Dioxirane in Flow.
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- Chemistry - A European Journal, 2019, v. 25, n. 5, p. 1203, doi. 10.1002/chem.201805657
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Across‐the‐World Automated Optimization and Continuous‐Flow Synthesis of Pharmaceutical Agents Operating Through a Cloud‐Based Server.
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- Angewandte Chemie, 2018, v. 130, n. 46, p. 15348, doi. 10.1002/ange.201809080
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Across‐the‐World Automated Optimization and Continuous‐Flow Synthesis of Pharmaceutical Agents Operating Through a Cloud‐Based Server.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 46, p. 15128, doi. 10.1002/anie.201809080
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Mimicking the surface and prebiotic chemistry of early Earth using flow chemistry.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04147-2
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Editorial: Harmonische Zusammenarbeit von Mensch und Maschine in der chemischen Synthese.
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- Angewandte Chemie, 2018, v. 130, n. 19, p. 5278, doi. 10.1002/ange.201802383
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The Engineering of Chemical Synthesis: Humans and Machines Working in Harmony.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 19, p. 5182, doi. 10.1002/anie.201802383
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- Article
A Versatile Route to Unstable Diazo Compounds via Oxadiazolines and their Use in Aryl-Alkyl Cross-Coupling Reactions.
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- Angewandte Chemie, 2017, v. 129, n. 52, p. 16829, doi. 10.1002/ange.201710445
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A Versatile Route to Unstable Diazo Compounds via Oxadiazolines and their Use in Aryl-Alkyl Cross-Coupling Reactions.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 52, p. 16602, doi. 10.1002/anie.201710445
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A Lewis Base Catalysis Approach for the Photoredox Activation of Boronic Acids and Esters.
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- Angewandte Chemie, 2017, v. 129, n. 47, p. 15332, doi. 10.1002/ange.201709690
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A Lewis Base Catalysis Approach for the Photoredox Activation of Boronic Acids and Esters.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 47, p. 15136, doi. 10.1002/anie.201709690
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A New Methodology for Incorporating Chiral Linkers into Stapled Peptides.
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- ChemBioChem, 2017, v. 18, n. 12, p. 1066, doi. 10.1002/cbic.201700075
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Rapid Asymmetric Synthesis of Disubstituted Allenes by Coupling of Flow-Generated Diazo Compounds and Propargylated Amines.
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- Angewandte Chemie, 2017, v. 129, n. 7, p. 1890, doi. 10.1002/ange.201611067
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Rapid Asymmetric Synthesis of Disubstituted Allenes by Coupling of Flow-Generated Diazo Compounds and Propargylated Amines.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 7, p. 1864, doi. 10.1002/anie.201611067
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Visible Light Activation of Boronic Esters Enables Efficient Photoredox C(sp<sup>2</sup>)-C(sp<sup>3</sup>) Cross-Couplings in Flow.
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- Angewandte Chemie, 2016, v. 128, n. 45, p. 14291, doi. 10.1002/ange.201605548
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Visible Light Activation of Boronic Esters Enables Efficient Photoredox C(sp<sup>2</sup>)-C(sp<sup>3</sup>) Cross-Couplings in Flow.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 45, p. 14085, doi. 10.1002/anie.201605548
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The Total Synthesis of the Bioactive Natural Product Plantazolicin A and Its Biosynthetic Precursor Plantazolicin B.
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- Chemistry - A European Journal, 2016, v. 22, n. 44, p. 15902, doi. 10.1002/chem.201603157
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Synthesis of Natural and Unnatural Cyclooligomeric Depsipeptides Enabled by Flow Chemistry.
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- Chemistry - A European Journal, 2016, v. 22, n. 12, p. 4206, doi. 10.1002/chem.201504457
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Callipeltosides A, B and C: Total Syntheses and Structural Confirmation.
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- Chemistry - A European Journal, 2015, v. 21, n. 38, p. 13261, doi. 10.1002/chem.201501877
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Back Cover: Callipeltosides A, B and C: Total Syntheses and Structural Confirmation (Chem. Eur. J. 38/2015).
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- Chemistry - A European Journal, 2015, v. 21, n. 38, p. 13464, doi. 10.1002/chem.201583804
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Maschinengestützte organische Synthese.
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- Angewandte Chemie, 2015, v. 127, n. 35, p. 10260, doi. 10.1002/ange.201501618
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Machine-Assisted Organic Synthesis.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 35, p. 10122, doi. 10.1002/anie.201501618
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A Versatile Room-Temperature Route to Di- and Trisubstituted Allenes Using Flow-Generated Diazo Compounds.
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- Angewandte Chemie, 2015, v. 127, n. 27, p. 8031, doi. 10.1002/ange.201501538
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- Article
A Versatile Room-Temperature Route to Di- and Trisubstituted Allenes Using Flow-Generated Diazo Compounds.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 27, p. 7920, doi. 10.1002/anie.201501538
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- Article
Facilitating Biomimetic Syntheses of Borrerine Derived Alkaloids by Means of Flow-Chemical Methods.
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- Australian Journal of Chemistry, 2015, v. 68, n. 4, p. 693, doi. 10.1071/CH14530
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Organische Synthese: Vormarsch der Maschinen.
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- Angewandte Chemie, 2015, v. 127, n. 11, p. 3514, doi. 10.1002/ange.201410744
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Organic Synthesis: March of the Machines.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 11, p. 3449, doi. 10.1002/anie.201410744
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Back Pressure Regulation of Slurry-Forming Reactions in Continuous Flow.
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- Chemical Engineering & Technology, 2015, v. 38, n. 2, p. 259, doi. 10.1002/ceat.201400445
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Total Syntheses of Linear Polythiazole/Oxazole Plantazolicin A and Its Biosynthetic Precursor Plantazolicin B.
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- Angewandte Chemie, 2015, v. 127, n. 4, p. 1300, doi. 10.1002/ange.201410063
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Total Syntheses of Linear Polythiazole/Oxazole Plantazolicin A and Its Biosynthetic Precursor Plantazolicin B.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 4, p. 1284, doi. 10.1002/anie.201410063
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A Systems Approach towards an Intelligent and Self-Controlling Platform for Integrated Continuous Reaction Sequences.
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- Angewandte Chemie, 2015, v. 127, n. 1, p. 146, doi. 10.1002/ange.201409356
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A Systems Approach towards an Intelligent and Self-Controlling Platform for Integrated Continuous Reaction Sequences.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 1, p. 144, doi. 10.1002/anie.201409356
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A General Continuous Flow Method for Palladium Catalysed Carbonylation Reactions Using Single and Multiple Tube-in-Tube Gas-Liquid Microreactors.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 29, p. 6418, doi. 10.1002/ejoc.201402804
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Flow Chemistry Meets Advanced Functional Materials.
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- Chemistry - A European Journal, 2014, v. 20, n. 39, p. 12348, doi. 10.1002/chem.201402801
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Synthesis of Riboflavines, Quinoxalinones and Benzodiazepines through Chemoselective Flow Based Hydrogenations.
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- Molecules, 2014, v. 19, n. 7, p. 9736, doi. 10.3390/molecules19079736
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Accelerating Spirocyclic Polyketide Synthesis using Flow Chemistry.
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- Angewandte Chemie, 2014, v. 126, n. 19, p. 5015, doi. 10.1002/ange.201402056
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Accelerating Spirocyclic Polyketide Synthesis using Flow Chemistry.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 19, p. 4915, doi. 10.1002/anie.201402056
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Flow-Based, Cerium Oxide Enhanced, Low-Level Palladium Sonogashira and Heck Coupling Reactions by Perovskite Catalysts.
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- Israel Journal of Chemistry, 2014, v. 54, n. 4, p. 371, doi. 10.1002/ijch.201300049
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Investigation of a Lithium-Halogen Exchange Flow Process for the Preparation of Boronates by Using a Cryo-Flow Reactor.
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- Chemistry - A European Journal, 2014, v. 20, n. 1, p. 263, doi. 10.1002/chem.201303736
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A Machine-Assisted Flow Synthesis of SR48692: A Probe for the Investigation of Neurotensin Receptor-1.
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- Chemistry - A European Journal, 2013, v. 19, n. 24, p. 7917, doi. 10.1002/chem.201300696
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Flow Microwave Technology and Microreactors in Synthesis.
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- Australian Journal of Chemistry, 2013, v. 66, n. 2, p. 2, doi. 10.1071/CH12365
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Flow Chemistry Syntheses of Styrenes, Unsymmetrical Stilbenes and Branched Aldehydes.
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- ChemCatChem, 2013, v. 5, n. 1, p. 159, doi. 10.1002/cctc.201200778
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Continuous flow reaction monitoring using an on-line miniature mass spectrometer.
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- Rapid Communications in Mass Spectrometry: RCM, 2012, v. 26, n. 17, p. 1999, doi. 10.1002/rcm.6312
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Convergent Total Syntheses of Callipeltosides A, B, and C.
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- Angewandte Chemie, 2012, v. 124, n. 37, p. 9500, doi. 10.1002/ange.201204868
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Convergent Total Syntheses of Callipeltosides A, B, and C.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 37, p. 9366, doi. 10.1002/anie.201204868
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On being green: Can flow chemistry help?
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- Chemical Record, 2012, v. 12, n. 4, p. 378, doi. 10.1002/tcr.201100041
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Asymmetric Homogeneous Hydrogenation in Flow using a Tube-in-Tube Reactor.
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- Advanced Synthesis & Catalysis, 2012, v. 354, n. 9, p. 1805, doi. 10.1002/adsc.201200073
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The Oxygen-Mediated Synthesis of 1,3-Butadiynes in Continuous Flow: Using Teflon AF-2400 to Effect Gas/Liquid Contact.
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- ChemSusChem, 2012, v. 5, n. 2, p. 274, doi. 10.1002/cssc.201100339
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