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Madani, Amiera, and Bartholomäus Pieber. “In Situ Reaction Monitoring in Photocatalytic Organic Synthesis.”10.1002/cctc.202201583__ChemCatChem, vol. 15, no. 7, e202201583, Wiley, 2023, doi:10.1002/cctc.202201583.

Murakami, Sho, et al. “Photocatalytic Cleavage of Trityl Protected Thiols and Alcohols.”10.1055/a-1979-5933__Synthesis, vol. 55, no. 09, Georg Thieme Verlag, 2023, pp. 1367–74, doi:10.1055/a-1979-5933.

Madani, Amiera, et al. “Visible-Light-Mediated Oxidative Debenzylation of 3-O-Benzyl-1,2:5,6-Di-O-Isopropylidene-;1-D-Glucofuranose.”10.15227/orgsyn.100.0271__Organic Syntheses, vol. 100, Organic Syntheses, 2023, pp. 271–86, doi:10.15227/orgsyn.100.0271.

Lepre, Enrico, et al. “Catalytic Properties of High Nitrogen Content Carbonaceous Materials.”10.1002/anie.202211663__Angewandte Chemie International Edition, vol. 62, no. 2, e202211663, Wiley, 2023, doi:10.1002/anie.202211663.

Næsborg, Line, et al. “Special Collection: Photocatalytic Synthesis.”10.1002/cctc.202300683__ChemCatChem, e202300683, Wiley, 2023, doi:10.1002/cctc.202300683.

Baunis, Haralds, and Bartholomäus Pieber. “Formal Radical Deoxyfluorination of Oxalate-Activated Alcohols Triggered by the Selectfluor-DMAP Charge-Transfer Complex.”10.1002/ejoc.202300769__European Journal of Organic Chemistry, vol. 26, no. 42, e202300769, Wiley, 2023, doi:10.1002/ejoc.202300769.

Traxler, Michael, et al. “Acridinefunctionalized Covalent Organic Frameworks (COFs) as Photocatalysts for Metallaphotocatalytic CN Crosscoupling.”10.1002/anie.202117738__Angewandte Chemie International Edition, vol. 61, no. 21, e202117738, Wiley, 2022, doi:10.1002/anie.202117738.

Madani, Amiera, et al. “Benzylic Fluorination Induced by a Charge-Transfer Complex with a Solvent-Dependent Selectivity Switch.”10.1021/acs.orglett.2c02050__Organic Letters, vol. 24, no. 29, American Chemical Society, 2022, pp. 5376–5380, doi:10.1021/acs.orglett.2c02050.

Cavedon, Cristian, et al. “Intraligand Charge Transfer Enables Visiblelightmediated Nickelcatalyzed Cross-Coupling Reactions.”10.1002/anie.202211433__Angewandte Chemie International Edition, vol. 61, no. 46, e202211433, Wiley, 2022, doi:10.1002/anie.202211433.

Zhao, Zhouxiang, et al. “Modulating the Surface and Photophysical Properties of Carbon Dots to Access Colloidal Photocatalysts for Cross-Couplings.”10.1021/acscatal.2c04025__ACS Catalysis, vol. 12, no. 22, American Chemical Society, 2022, pp. 13831–37, doi:10.1021/acscatal.2c04025.

Schmermund, Luca, et al. “Chromoselective Photocatalysis Enables Stereocomplementary Biocatalytic Pathways.”10.1002/anie.202100164__Angewandte Chemie International Edition, vol. 60, no. 13, Wiley, 2021, pp. 6965–69, doi:10.1002/anie.202100164.

Reischauer, Susanne, and Bartholomäus Pieber. “Recyclable, Bifunctional Metallaphotocatalysts for CS Crosscoupling Reactions.”10.1002/cptc.202100062__ChemPhotoChem, vol. 5, no. 8, Wiley, 2021, pp. 716–20, doi:10.1002/cptc.202100062.

Zhao, Zhouxiang, et al. “Carbon Dot/TiO Nanocomposites as Photocatalysts for Metallaphotocatalytic Carbon-Heteroatom Cross-Couplings.”10.1039/d1gc01284c__Green Chemistry, vol. 23, no. 12, Royal Society of Chemistry, 2021, pp. 4524–30, doi:10.1039/d1gc01284c.

Reischauer, Susanne, and Bartholomäus Pieber. “Emerging Concepts in Photocatalytic Organic Synthesis.”10.1016/j.isci.2021.102209__IScience, vol. 24, no. 3, 102209, Elsevier, 2021, doi:10.1016/j.isci.2021.102209.

Cavedon, Cristian, et al. “Visible-Light-Mediated Oxidative Debenzylation Enables the Use of Benzyl Ethers as Temporary Protecting Groups.”10.1021/acs.orglett.0c04026__Organic Letters, vol. 23, no. 2, American Chemical Society, 2021, pp. 514–18, doi:10.1021/acs.orglett.0c04026.

Schmermund, Luca, et al. Switching between Enantiomers by Combining Chromoselective Photocatalysis and Biocatalysis. ChemRxiv, doi:10.26434/chemrxiv.13521527.

Cavedon, Cristian, et al. Photocatalyst-Free, Visible-Light-Mediated Nickel Catalyzed Carbon–Heteroatom Cross-Couplings. ChemRxiv, doi:10.26434/chemrxiv-2021-kt2wr.

Reischauer, Susanne, et al. “Modular, Self-Assembling Metallaphotocatalyst for Cross-Couplings Using the Full Visible-Light Spectrum.”10.1021/acscatal.0c03950__ACS Catalysis, vol. 10, no. 22, American Chemical Society, 2020, pp. 13269–13274, doi:10.1021/acscatal.0c03950.

Cavedon, Cristian, et al. “Photochemical Strategies for Carbon–Heteroatom Bond Formation.”10.1002/ejoc.201901173__European Journal of Organic Chemistry, vol. 2020, no. 10, Wiley, 2020, pp. 1379–92, doi:10.1002/ejoc.201901173.

Gisbertz, Sebastian, and Bartholomäus Pieber. “Heterogeneous Photocatalysis in Organic Synthesis.”10.1002/cptc.202000137__ChemPhotoChem, vol. 4, no. 7, Wiley, 2020, pp. 454–454, doi:10.1002/cptc.202000137.

Malik, Jamal A., et al. “Evidence for Photocatalyst Involvement in Oxidative Additions of Nickel-Catalyzed Carboxylate O-Arylations.”10.1021/jacs.0c02848__Journal of the American Chemical Society, vol. 142, no. 25, American Chemical Society, 2020, pp. 11042–49, doi:10.1021/jacs.0c02848.

Mazzanti, Stefano, et al. “Dichloromethylation of Enones by Carbon Nitride Photocatalysis.”10.1038/s41467-020-15131-0__Nature Communications, vol. 11, 1387, Springer Nature, 2020, doi:10.1038/s41467-020-15131-0.

Gisbertz, Sebastian, et al. “Overcoming Limitations in Dual Photoredox/Nickel-Catalysed C–N Cross-Couplings Due to Catalyst Deactivation.”10.1038/s41929-020-0473-6__Nature Catalysis, vol. 3, no. 8, Springer Nature, 2020, pp. 611–20, doi:10.1038/s41929-020-0473-6.

Rosso, Cristian, et al. “An Oscillatory Plug Flow Photoreactor Facilitates Semi-Heterogeneous Dual Nickel/Carbon Nitride Photocatalytic C–N Couplings.”10.1039/d0re00036a__Reaction Chemistry and Engineering, vol. 5, no. 3, Royal Society of Chemistry, 2020, pp. 597–604, doi:10.1039/d0re00036a.

Pieber, Bartholomäus, et al. “Semiheterogeneous Dual Nickel/Photocatalysis Using Carbon Nitrides: Esterification of Carboxylic Acids with Aryl Halides.”10.1002/anie.201902785__Angewandte Chemie International Edition, vol. 58, no. 28, Wiley, 2019, pp. 9575–80, doi:10.1002/anie.201902785.

Guberman, Mónica, et al. “Safe and Scalable Continuous Flow Azidophenylselenylation of Galactal to Prepare Galactosamine Building Blocks.”10.1021/acs.oprd.9b00456__Organic Process Research and Development, vol. 23, no. 12, American Chemical Society, 2019, pp. 2764–70, doi:10.1021/acs.oprd.9b00456.

Cavedon, Cristian, et al. “Semiheterogeneous Dual Nickel/Photocatalytic (Thio)Etherification Using Carbon Nitrides.”10.1021/acs.orglett.9b01957__Organic Letters, vol. 21, no. 13, American Chemical Society, 2019, pp. 5331–34, doi:10.1021/acs.orglett.9b01957.

Pieber, Bartholomäus, et al. “Continuous Heterogeneous Photocatalysis in Serial Micro-Batch Reactors.”10.1002/anie.201712568__Angewandte Chemie International Edition, vol. 57, no. 31, Wiley, 2018, pp. 9976–79, doi:10.1002/anie.201712568.

Plutschack, Matthew B., et al. “The Hitchhiker’s Guide to Flow Chemistry.”10.1021/acs.chemrev.7b00183__Chemical Reviews, vol. 117, no. 18, American Chemical Society, 2017, pp. 11796–893, doi:10.1021/acs.chemrev.7b00183.

Pieber, Bartholomäus, et al. “Integrated Flow Processing - Challenges in Continuous Multistep Synthesis.”10.1556/1846.2017.00016__Journal of Flow Chemistry, vol. 7, no. 3–4, AKJournals, 2017, pp. 129–36, doi:10.1556/1846.2017.00016.

Pieber, Bartholomäus, et al. “Selective Olefin Reduction in Thebaine Using Hydrazine Hydrate and O under Intensified Continuous Flow Conditions.”10.1021/acs.oprd.5b00370__Organic Process Research and Development, vol. 20, no. 2, American Chemical Society, 2016, pp. 376–85, doi:10.1021/acs.oprd.5b00370.

Pieber, Bartholomäus, and C. Oliver Kappe. “Generation and Synthetic Application of Trifluoromethyl Diazomethane Utilizing Continuous Flow Technologies.”10.1021/acs.orglett.6b00194__Organic Letters, vol. 18, no. 5, American Chemical Society, 2016, pp. 1076–79, doi:10.1021/acs.orglett.6b00194.

Kappe, C., et al. “Continuous Synthesis of Hydantoins: Intensifying the Bucherer–Bergs Reaction.”10.1055/s-0035-1560317__Synlett, vol. 27, no. 01, Georg Thieme Verlag, 2016, pp. 83–87, doi:10.1055/s-0035-1560317.

Pieber, Bartholomäus, et al. “Continuous Flow Reduction of Artemisinic Acid Utilizing Multi-Injection Strategies-Closing the Gap towards a Fully Continuous Synthesis of Antimalarial Drugs.”10.1002/chem.201406439__Chemistry - A European Journal, vol. 21, no. 11, Wiley, 2015, pp. 4368–76, doi:10.1002/chem.201406439.

Salvador, Carlos Eduardo M., et al. “A Sequential Ugi Multicomponent/Cu-Catalyzed Azide–Alkyne Cycloaddition Approach for the Continuous Flow Generation of Cyclic Peptoids.”10.1021/acs.joc.5b00445__The Journal of Organic Chemistry, vol. 80, no. 9, American Chemical Society, 2015, pp. 4590–602, doi:10.1021/acs.joc.5b00445.

Pieber, Bartholomäus, and C. Oliver Kappe. “Aerobic Oxidations in Continuous Flow.”10.1007/3418_2015_133__Organometallic Flow Chemistry, edited by Timothy Noël, 1st ed., vol. 57, Springer Nature, 2015, pp. 97–136, doi:10.1007/3418_2015_133.

Hofbauer, Harald F., et al. “Regulation of Gene Expression through a Transcriptional Repressor That Senses Acyl-Chain Length in Membrane Phospholipids.”10.1016/j.devcel.2014.04.025__Developmental Cell, vol. 29, no. 6, Elsevier, 2014, pp. 9-739, doi:10.1016/j.devcel.2014.04.025.

Moghaddam, Mojtaba Mirhosseini, et al. “Immobilized Iron Oxide Nanoparticles as Stable and Reusable Catalysts for Hydrazine-Mediated Nitro Reductions in Continuous Flow.”10.1002/cssc.201402455__ChemSusChem, vol. 7, no. 11, Wiley, 2014, pp. 3122–31, doi:10.1002/cssc.201402455.

Pieber, Bartholomäus, et al. “Flash Carboxylation: Fast Lithiation–Carboxylation Sequence at Room Temperature in Continuous Flow.”10.1039/c4ra01442a__RSC Advances, vol. 4, no. 26, 13430, Royal Society of Chemistry, 2014, doi:10.1039/c4ra01442a.

Pieber, Bartholomäus, et al. “In Situ Generation of Diimide from Hydrazine and Oxygen: Continuous-Flow Transfer Hydrogenation of Olefins.”10.1002/anie.201303528__Angewandte Chemie International Edition, vol. 52, no. 39, Wiley, 2013, pp. 10241–44, doi:10.1002/anie.201303528.

Kappe, C. Oliver, et al. “Microwave Effects in Organic Synthesis: Myth or Reality?”10.1002/anie.201204103__Angewandte Chemie International Edition, vol. 52, no. 4, Wiley, 2013, pp. 1088–94, doi:10.1002/anie.201204103.

Pieber, Bartholomäus, and C. Oliver Kappe. “Direct Aerobic Oxidation of 2-Benzylpyridines in a Gas-Liquid Continuous-Flow Regime Using Propylene Carbonate as a Solvent.”10.1039/c2gc36896j__Green Chemistry, vol. 15, no. 2, Royal Society of Chemistry, 2013, pp. 320–24, doi:10.1039/c2gc36896j.

Pieber, Bartholomäus, et al. “Direct Arylation of Benzene with Aryl Bromides Using Hightemperature/Highpressure Process Windows: Expanding the Scope of C-H Activation Chemistry.”10.1002/chem.201103748__Chemistry – A European Journal, vol. 18, no. 16, Wiley, 2012, pp. 5047–55, doi:10.1002/chem.201103748.

Kumar, G. Sathish, et al. “Copper-Catalyzed Formation of C-O Bonds by Direct ;1-C-H Bond Activation of Ethers Using Stoichiometric Amounts of Peroxide in Batch and Continuous-Flow Formats.”10.1002/chem.201200815__Chemistry - A European Journal, vol. 18, no. 20, Wiley, 2012, pp. 6124–28, doi:10.1002/chem.201200815.

Pieber, Bartholomäus, et al. “Novel Sensitive Determination of Steryl Glycosides in Biodiesel by Gas Chromatography-Mass Spectroscopy.”10.1016/j.chroma.2010.08.006__Journal of Chromatography A, vol. 1217, no. 42, Elsevier, 2010, pp. 6555–61, doi:10.1016/j.chroma.2010.08.006.