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