Meno a priezvisko:
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Mgr. Samuel Andrejčák
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Typ dokumentu:
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Vedecko/umelecko-pedagogická charakteristika osoby
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Názov vysokej školy:
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Univerzita Komenského v Bratislave
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Sídlo vysokej školy:
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Šafárikovo námestie 6, 818 06 Bratislava
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V.1.a - Názov profilového predmetu | V.1.b - Študijný program | V.1.c - Stupeň | V.1.d - Študijný odbor |
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Chemické modelovanie | Chémia, Biochémia | I. | Chémia |
Cvičenie z organickej chémie 1 | Chémia, Biochémia | I | Chémia |
V.5.a - Názov predmetu | V.5.b - Študijný program | V.5.c - Stupeň | V.5.d - Študijný odbor |
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Cvičenie z organickej chémie pre biológov | Biológia | I. | Biológia |
S. Andrejčák, M. Májek, Chem. – A Eur. J. 2024, 30, e202401795. Applications of Electrophotocatalysis in C−H Functionalization of Organic Molecules, https://doi.org/10.1002/chem.202401795.
S. Andrejčák, P. Kisszékelyi, M. Májek, R. Šebesta, European J. Org. Chem. 2023, 26, e202201399. Mechanochemical Radical Boronation of Aryl Diazonium Salts Promoted by Sodium Chloride, https://doi.org/10.1002/ejoc.202201399.
T. Čarný, T. Peňaška, S. Andrejčák, R. Šebesta, Chem. – A Eur. J. 2022, 28, e202202040; Mechanochemical Pd-Catalyzed Cross-Coupling of Arylhalides and Organozinc Pivalates; https://doi.org/10.1002/chem.202202040.
K. Plevová, P. Kisszékelyi, D. Vargová, S. Andrejčák, V. Tóth, L. Fertáľ, E. Rakovský, J. Filo, R. Šebesta, Chem. – A Eur. J. 2021, 27, 15501–15507. Diastereoselective Double C−H Functionalization of Chiral Ferrocenes with Heteroaromatics; https://doi.org/10.1002/chem.202102624.
M. Žabka, A. Kocian, S. Bilka, S. Andrejčák, R. Šebesta, European J. Org. Chem. 2019, 2019, 6077–6087. Transformation of Racemic Azlactones into Enantioenriched Dihydropyrroles and Lactones Enabled by Hydrogen-Bond Organocatalysis; https://doi.org/10.1002/ejoc.201901052.
S. Andrejčák, M. Májek, Chem. – A Eur. J. 2024, 30, e202401795. Applications of Electrophotocatalysis in C−H Functionalization of Organic Molecules, https://doi.org/10.1002/chem.202401795.
S. Andrejčák, P. Kisszékelyi, M. Májek, R. Šebesta, European J. Org. Chem. 2023, 26, e202201399. Mechanochemical Radical Boronation of Aryl Diazonium Salts Promoted by Sodium Chloride, https://doi.org/10.1002/ejoc.202201399.
T. Čarný, T. Peňaška, S. Andrejčák, R. Šebesta, Chem. – A Eur. J. 2022, 28, e202202040; Mechanochemical Pd-Catalyzed Cross-Coupling of Arylhalides and Organozinc Pivalates; https://doi.org/10.1002/chem.202202040.
K. Plevová, P. Kisszékelyi, D. Vargová, S. Andrejčák, V. Tóth, L. Fertáľ, E. Rakovský, J. Filo, R. Šebesta, Chem. – A Eur. J. 2021, 27, 15501–15507. Diastereoselective Double C−H Functionalization of Chiral Ferrocenes with Heteroaromatics; https://doi.org/10.1002/chem.202102624.
M. Žabka, A. Kocian, S. Bilka, S. Andrejčák, R. Šebesta, European J. Org. Chem. 2019, 2019, 6077–6087. Transformation of Racemic Azlactones into Enantioenriched Dihydropyrroles and Lactones Enabled by Hydrogen-Bond Organocatalysis; https://doi.org/10.1002/ejoc.201901052.
S. Andrejčák, P. Kisszékelyi, M. Májek, R. Šebesta, European J. Org. Chem. 2023, 26, e202201399. Mechanochemical Radical Boronation of Aryl Diazonium Salts Promoted by Sodium Chloride, https://doi.org/10.1002/ejoc.202201399.
Cited in:
Y. Zhao, Z. Yang, X. Wang, Q. Kang, B. Wang, T. Wu, H. Lei, P. Ma, W. Su, S. Wang, Z. Wu, X. Huang, C. Fan, X. Wei, Adv. Sci. 2024, 11, 2404071. Mechanochemical Synthesis of α-halo Alkylboronic Esters; https://doi.org/10.1002/advs.202404071
T. Čarný, T. Peňaška, S. Andrejčák, R. Šebesta, Chem. – A Eur. J. 2022, 28, e202202040; Mechanochemical Pd-Catalyzed Cross-Coupling of Arylhalides and Organozinc Pivalates; https://doi.org/10.1002/chem.202202040.
Cited in:
S. Yang, X. Yu, Y. Liu, M. Tomasini, L. Caporaso, A. Poater, L. Cavallo, C. S. J. Cazin, S. P. Nolan, M. Szostak, J. Org. Chem. 2023, 88, 10858–10868. Suzuki–Miyaura Cross-Coupling of Amides by N–C Cleavage Mediated by Air-Stable, Well-Defined [Pd(NHC)(sulfide)Cl2] Catalysts: Reaction Development, Scope, and Mechanism; https://doi.org/10.1021/acs.joc.3c00912.
K. Plevová, P. Kisszékelyi, D. Vargová, S. Andrejčák, V. Tóth, L. Fertáľ, E. Rakovský, J. Filo, R. Šebesta, Chem. – A Eur. J. 2021, 27, 15501–15507. Diastereoselective Double C−H Functionalization of Chiral Ferrocenes with Heteroaromatics; https://doi.org/10.1002/chem.202102624.
Cited in:
A. Mori, S. Curpanen, C. Pezzetta, A. Perez-Luna, G. Poli, J. Oble, European J. Org. Chem. 2022, 2022, e202200727. C−H Activation Based Functionalization of Furfural Derivatives; https://doi.org/10.1002/ejoc.202200727
M. Žabka, A. Kocian, S. Bilka, S. Andrejčák, R. Šebesta, European J. Org. Chem. 2019, 2019, 6077–6087. Transformation of Racemic Azlactones into Enantioenriched Dihydropyrroles and Lactones Enabled by Hydrogen-Bond Organocatalysis; https://doi.org/10.1002/ejoc.201901052.
Cited in:
P. Ruan, C. Zhang, J. Wu, F. Xiao, Y. Zhang, Q. Tan, Z. Su, X. Feng, X. Liu, Chem. Commun. 2023, 59, 8250–8253. Asymmetric [3+2]-cyclization of α-imino amide surrogates to construct 3,4-diaminopyrrolidine-2,5-diones; https://doi.org/10.1039/D3CC01203D.