Publications:

[21]:„Mechanochemical Radical Boronation of Aryl Diazonium Salts Promoted by Sodium Chloride“
Andrejčák S., Kisszékelyi P., Májek M.*, Šebesta R.*; Eur. J. Org. Chem 2023, 26, e202201399, DOI: 10.1002/ejoc.202201399

[20]:„How to Harness Electrochemical Mediators for Photocatalysis – A Systematic Approach Using the Phenanthro[9,10‐d]imidazole Framework as a Test Case“
Enders P., Májek M.*, Lam C. M., Little R. D. L.*, Francke R.*; ChemCatChem 2023, 15, e202200830, DOI: 10.1002/cctc.202200830

[19]:„Deracemization of Binaphthyl by Suzuki Diarylation: The Role of Electronic and Steric Effects“
Bulko F., Májek M., Putala M.; J. Org. Chem. 2022, 87, 9316, DOI: 10.1021/acs.joc.2c01041

[18]:„Mediated Electron Transfer in Electrosynthesis: Concepts, Applications, and Recent Influences from Photoredox Catalysis“ in
Francke R., Májek M.; in Sustainable and Functional Redox Chemistry (ed. Inagi, S.) 2022, RSC, DOI: 10.1039/9781839164828

[17]: „Reaction Outcome Critically Dependent on the Method of Workup: An Example from the Synthesis of 1-Isoquinolones“
Matouš P., Májek M., Kysilka O., Kuneš J., Maříková J., Růžička A., Pour M., Kočovský P.; J. Org. Chem. 2021, 86, 8076, DOI: 10.1021/acs.joc.1c00561

[16]: „Phosphate linkers with traceable cyclic intermediates for self-immolation detection and monitoring“
Procházková E., Šimon P., Straka M., Filo J., Májek M., Cigáň M., Baszczyňski O.; Chem. Commun. 2021, 57, 211, DOI: 10.1039/D0CC06928K

[15]: „Aryl Pyrazoles from Photocatalytic Cycloadditions of Arenediazonium“
Cardinale L., Neumeier M., Májek M.*, Jacobi von Wangelin A.*; Org. Lett. 2020, 22, 7219, DOI: 10.1021/acs.orglett.0c02514

[14]: „The Electrochemically Catalyzed Newman-Kwart Rearrangement: Mechanism, Structure-Reactivity Relationship, and Parallels to Photoredox Catalysis“
Roesel A. F., Ugandi M., Huyen N. T. T., Májek M., Broese T., Roemelt M., Francke R.; J. Org. Chem.  2020, 85, 8029, DOI: 10.1021/acs.joc.0c00831

[13]: „Visible light-mediated photo-oxygenation of arylcyclohexenes“
Bayer P., Schachtner J., Májek M., Jacobi von Wangelin A.; Org. Chem. Front. 2019, 6, 2877, DOI: 10.1039/C9QO00493A

[12]: „Iodophenylsulfonates and Iodobenzoates as Redox‐Active Supporting Electrolytes for Electrosynthesis“
Roesel A. F., Broese T., Májek M., Francke R.; ChemElectroChem 2019, 6, 4229, DOI: 10.1002/celc.201900540

[11]: „Dichromatic Photocatalytic Substitutions of Aryl Halides with a Small Organic Dye“
Neumeier M., Sampedro D., Májek M., de la Peña O’Shea V. A., Jacobi von Wangelin A., Pérez-Ruiz R.; Chem. Eur. J. 2018, 24, 105, DOI: 10.1002/chem.201705326

[10]:  „Radical Aromatic Trifluoromethylthiolation: Photoredox Catalysis vs. Base Mediation”
Koziakov D., Májek M., Jacobi von Wangelin J.; Eur. J. Org. Chem. 2017, 6722, DOI: 10.1002/ejoc.201701339

[9]: „Aromatic Chlorosulfonylation by Photoredox Catalysis”
Májek M., Neumeier M., Jacobi von Wangelin A.; ChemSusChem 2017, 10, 151, DOI: 10.1002/cssc.201601293

[8]:  „Metal-free radical thiolations mediated by very weak bases”
Koziakov D., Májek M., Jacobi von Wangelin A.; Org. Biomol. Chem.  2016, 14, 11347, DOI: 10.1039/C6OB02276F

[7]: „Mechanistic Perspectives on Organic Photoredox Catalysis for Aromatic Substitutions”
Májek M., Jacobi von Wangelin A.; Acc. Chem. Res. 2016, 49, 2316, DOI: 10.1021/acs.accounts.6b00293

from PhD studies:

[6]:  „Application of Visible-to-UV Photon Upconversion to Photoredox Catalysis: The Activation of Aryl Bromides”
Májek M.; Faltermeier U.; Dick B.; Pérez-Ruiz R.; Jacobi von Wangelin A.; Chem. Eur. J. 2015, 21, 15496, DOI: 10.1002/chem.201502698
– selected as a VIP paper by reviewers

[5]: „Visible Light Driven Hydro-/Deutero- defunctionalization of Anilines”
Májek M.; Filace F.; Jacobi von Wangelin A.; Chem. Eur. J. 2015, 21, 4518, DOI: 10.1002/chem.201406461

[4]:  „Metal-Free Carbonylations by Photoredox Catalysis”
Májek M., Jacobi von Wangelin A.; Angew. Chem. Int. Ed. 2015, 54, 2270.
– selected as a hot paper by reviewers; featured in Synform 2015, 8, A102; featured in Synfacts 2015, 11(2), 0199; featured in Nachr. Chem. 2015, 63(6), 620, DOI: 10.1002/anie.201408516

[3]:  „On the mechanism of photocatalytic reactions with eosin Y”
Májek M.*; Filace F.; Jacobi von Wangelin A.*; Beilstein J. Org. Chem. 2014, 10, 981, DOI: 10.3762/bjoc.10.97

[2]: „Ambient-Light-Mediated Copper-Catalyzed C-C and C-N Bond Formation”
Májek M.; Jacobi von Wangelin A.; Angew. Chem. Int. Ed. 2013, 52, 5919, DOI: 10.1002/anie.201301843

[1]: „Organocatalytic visible light mediated synthesis of aryl sulfides”
Májek M.; Jacobi von Wangelin A.; “ Chem. Commun. 2013, 49, 5507, DOI: 10.1039/C3CC41867G