@article{MTMT:32729488,
	title = {Development and Process Intensification of an Efficient Flow–Cascade Reaction Sequence in the Synthesis of Afizagabar},
	url = {https://m2.mtmt.hu/api/publication/32729488},
	author = {Pethő, Bálint and Szilágyi, Gábor B. and Mengyel, Béla and Nagy, Tamás and Farkas, Ferenc and Kátainé Fadgyas, Katalin and Volk, Balázs},
	doi = {10.1021/acs.oprd.1c00481},
	journal-iso = {ORG PROCESS RES DEV},
	journal = {ORGANIC PROCESS RESEARCH & DEVELOPMENT},
	volume = {26},
	unique-id = {32729488},
	issn = {1083-6160},
	year = {2022},
	eissn = {1520-586X},
	pages = {1223-1235},
	orcid-numbers = {Volk, Balázs/0000-0002-2019-1874}
}

@misc{MTMT:33106268,
	title = {Az afizagabar gyógyszerjelölt molekula kulcsintermedierjének négylépéses áramlásos-kaszkád előállítása és az eljárás méretnövelése},
	url = {https://m2.mtmt.hu/api/publication/33106268},
	author = {Pethő, Bálint and Szilágyi, Gábor and Mengyel, Béla and Nagy, Tamás and Kátainé Fadgyas, Katalin and Volk, Balázs},
	unique-id = {33106268},
	year = {2022},
	orcid-numbers = {Volk, Balázs/0000-0002-2019-1874}
}

@article{MTMT:30428919,
	title = {Synthesis of Aryl- and Heteroaryl-trifluoroethyl Ethers: Aims, Challenges and New Methodologies},
	url = {https://m2.mtmt.hu/api/publication/30428919},
	author = {Pethő, Bálint and Novák, Zoltán},
	doi = {10.1002/ajoc.201800414},
	journal-iso = {ASIAN J ORG CHEM},
	journal = {ASIAN JOURNAL OF ORGANIC CHEMISTRY},
	volume = {8},
	unique-id = {30428919},
	issn = {2193-5807},
	year = {2019},
	eissn = {2193-5815},
	pages = {568-575},
	orcid-numbers = {Novák, Zoltán/0000-0001-5525-3070}
}

@article{MTMT:30773928,
	title = {Development of palladium-catalyzed cross-coupling reactions for carbon-carbon and carbon-heteroatom bond forming reactions of aryl chlorides},
	url = {https://m2.mtmt.hu/api/publication/30773928},
	author = {Novák, Zoltán and Pethő, Bálint and Vangel, Dora and Zwillinger, Márton and Csenki, Janos and Tolnai, Gergely László and Ondi, Levente},
	journal-iso = {ABSTR PAP AM CHEM S},
	journal = {ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY},
	volume = {257},
	unique-id = {30773928},
	issn = {0065-7727},
	year = {2019},
	pages = {325-326},
	orcid-numbers = {Novák, Zoltán/0000-0001-5525-3070; Tolnai, Gergely László/0000-0002-5253-5117}
}

@mastersthesis{MTMT:31149635,
	title = {Szén-oxigén kötés kialakítása palládiumkatalizált kapcsolási reakciókban},
	url = {https://m2.mtmt.hu/api/publication/31149635},
	author = {Pethő, Bálint},
	doi = {10.15476/ELTE.2019.030},
	publisher = {Eötvös Loránd University},
	unique-id = {31149635},
	year = {2019}
}

@article{MTMT:3397114,
	title = {Palladium catalyzed chloroethoxylation of aromatic and heteroaromatic chlorides: An orthogonal functionalization of a chloroethoxy linker},
	url = {https://m2.mtmt.hu/api/publication/3397114},
	author = {Pethő, Bálint and Vangel, D and Csenki, János Tivadar and Zwillinger, Márton and Novák, Zoltán},
	doi = {10.1039/c8ob01146j},
	journal-iso = {ORG BIOMOL CHEM},
	journal = {ORGANIC & BIOMOLECULAR CHEMISTRY},
	volume = {16},
	unique-id = {3397114},
	issn = {1477-0520},
	keywords = {Chemistry; ETHERS; ARYL HALIDES; REDUCTIVE ELIMINATION; CROSS-COUPLING REACTIONS; Iodides; arylation; PRIMARY ALCOHOLS; Trifluoromethylation; C-O BOND},
	year = {2018},
	eissn = {1477-0539},
	pages = {4895-4899},
	orcid-numbers = {Novák, Zoltán/0000-0001-5525-3070}
}

@article{MTMT:3273433,
	title = {Palladium Catalyzed 2,2,2-Trifluoroethoxylation of Aromatic and Heteroaromatic Chlorides Utilizing Borate Salt and the Synthesis of Trifluoro Analog of Sildenafil},
	url = {https://m2.mtmt.hu/api/publication/3273433},
	author = {Pethő, Bálint and Zwillinger, Márton and Csenki, János Tivadar and Káncz, Anna and Krámos, Balázs and Müller, Judit and Balogh, György Tibor and Novák, Zoltán},
	doi = {10.1002/chem.201704205},
	journal-iso = {CHEM-EUR J},
	journal = {CHEMISTRY-A EUROPEAN JOURNAL},
	volume = {23},
	unique-id = {3273433},
	issn = {0947-6539},
	abstract = {A simple and convenient method was developed for the introduction of 2,2,2-trifluoroethoxy group to various aromatic and heteroaromatic systems. The novel process utilizes aromatic chlorides as substrates, and tetrakis(2,2,2-trifluoroethoxy) borate salt as an inexpensive and readily available fluoroalkoxy source in a palladium-catalyzed cross coupling reaction. The power of the developed methodology was demonstrated in the synthesis of fluorous derivative of Sildenafil.},
	keywords = {PALLADIUM; borates; Trifluoroethoxylation},
	year = {2017},
	eissn = {1521-3765},
	pages = {15628-15632},
	orcid-numbers = {Balogh, György Tibor/0000-0003-3347-1880; Novák, Zoltán/0000-0001-5525-3070}
}

@article{MTMT:2504667,
	title = {Palladium-Catalyzed Methoxylation of Aromatic Chlorides with Borate Salts},
	url = {https://m2.mtmt.hu/api/publication/2504667},
	author = {Tolnai, Gergely László and Pethő, Bálint and Králl, Péter and Novák, Zoltán},
	doi = {10.1002/adsc.201300687},
	journal-iso = {ADV SYNTH CATAL},
	journal = {ADVANCED SYNTHESIS & CATALYSIS},
	volume = {356},
	unique-id = {2504667},
	issn = {1615-4150},
	abstract = {Herein we disclose a simple palladium-catalyzed transformation for the methoxylation of aromatic chlorides with tetramethoxyborate salts. The procedure provides a new and efficient synthetic tool for the introduction of a methoxy group into aromatic systems. In addition, the reaction can be achieved using a wide range of aromatic and heteroaromatic chlorides, the cheapest class of halides.},
	keywords = {PALLADIUM; borates; cross-coupling; Lewis acids},
	year = {2014},
	eissn = {1615-4169},
	pages = {125-129},
	orcid-numbers = {Tolnai, Gergely László/0000-0002-5253-5117; Novák, Zoltán/0000-0001-5525-3070}
}

@article{MTMT:2238974,
	title = {Iron-surfactant nanocomposite-catalyzed benzylic oxidation in water},
	url = {https://m2.mtmt.hu/api/publication/2238974},
	author = {Szabó, Fruzsina and Pethő, Bálint and Gonda, Zsombor and Novák, Zoltán},
	doi = {10.1039/C3RA22856H},
	journal-iso = {RSC ADV},
	journal = {RSC ADVANCES},
	volume = {3},
	unique-id = {2238974},
	issn = {2046-2069},
	abstract = {Benzylic oxidation in the presence of an iron-surfactant nanocomposite catalyst under aqueous conditions is described. A significant reaction rate acceleration in the presence of anionic surfactants was demonstrated. Several benzylic substrates were efficiently transformed to ketones under mild conditions.},
	year = {2013},
	eissn = {2046-2069},
	pages = {4903-4908},
	orcid-numbers = {Gonda, Zsombor/0000-0001-9843-5907; Novák, Zoltán/0000-0001-5525-3070}
}