@article{MTMT:31365295,
	title = {Steroidal ferrocenes as potential enzyme inhibitors of the estrogen biosynthesis},
	url = {https://m2.mtmt.hu/api/publication/31365295},
	author = {Herman, Bianka Edina and Gardi, János and Julesz, János and Tömböly, Csaba and Szánti-Pintér, Eszter and Fehér, Klaudia and Skodáné Földes, Rita and Szécsi, Mihály},
	doi = {10.1007/s42977-020-00023-7},
	journal-iso = {BIOL FUTURA},
	journal = {BIOLOGIA FUTURA},
	volume = {71},
	unique-id = {31365295},
	issn = {2676-8615},
	year = {2020},
	eissn = {2676-8607},
	pages = {249-264},
	orcid-numbers = {Szánti-Pintér, Eszter/0000-0001-8263-9884; Skodáné Földes, Rita/0000-0002-9810-1509; Szécsi, Mihály/0000-0002-4272-1362}
}

@mastersthesis{MTMT:30982307,
	title = {Rézkatalizált azid-alkin cikloaddíció: szintézis és katalizátorfejlesztés},
	url = {https://m2.mtmt.hu/api/publication/30982307},
	author = {Fehér, Klaudia},
	doi = {10.18136/PE.2018.692},
	publisher = {University of Pannonia},
	unique-id = {30982307},
	year = {2018}
}

@mastersthesis{MTMT:30982300,
	title = {Réz-katalizált azid-alkin cikloaddíció: szintézis és katalizátorfejlesztés},
	url = {https://m2.mtmt.hu/api/publication/30982300},
	author = {Fehér, Klaudia},
	unique-id = {30982300},
	year = {2018}
}

@article{MTMT:3400511,
	title = {Heterogeneous azide-alkyne cycloaddition in the presence of a copper catalyst supported on an ionic liquid polymer/silica hybrid material},
	url = {https://m2.mtmt.hu/api/publication/3400511},
	author = {Fehér, Klaudia and Nagy, Enikő and Szabo, P and Yuzhakova, Tatiana and Srankó, Dávid Ferenc and Gömöry, Ágnes and Kollár, László and Skodáné Földes, Rita},
	doi = {10.1002/aoc.4343},
	journal-iso = {APPL ORGANOMET CHEM},
	journal = {APPLIED ORGANOMETALLIC CHEMISTRY},
	volume = {32},
	unique-id = {3400511},
	issn = {0268-2605},
	year = {2018},
	eissn = {1099-0739},
	orcid-numbers = {Gömöry, Ágnes/0000-0001-5216-0135; Skodáné Földes, Rita/0000-0002-9810-1509}
}

@article{MTMT:2940107,
	title = {A modular synthesis of 1,4,5-trisubstituted 1,2,3-triazoles with ferrocene moieties},
	url = {https://m2.mtmt.hu/api/publication/2940107},
	author = {Fehér, Klaudia and Gömöry, Ágnes and Skodáné Földes, Rita},
	doi = {10.1007/s00706-015-1490-z},
	journal-iso = {MONATSH CHEM},
	journal = {MONATSHEFTE FUR CHEMIE},
	volume = {146},
	unique-id = {2940107},
	issn = {0026-9247},
	abstract = {Regioselective synthesis of 1,2,3-triazoles with ferrocenyl moieties in positions 1, 4, and 5 was carried out in a two-step reaction sequence: a copper-mediated azide-alkyne cycloaddition followed by a palladium-catalyzed cross-coupling. A new route towards 5-iodo-1,2,3-triazoles was developed using N-iodomorpholine hydrogen iodide, instead of the corrosive and toxic ICl, as the I+ source. The novel methodology together with a consecutive Suzuki or Sonogashira reaction was shown to be a useful procedure for the synthesis of a wide range of ferrocenyl 1,2,3-triazoles with di- and triferrocenyl derivatives among them.},
	year = {2015},
	eissn = {1434-4475},
	pages = {1455-1463},
	orcid-numbers = {Gömöry, Ágnes/0000-0001-5216-0135; Skodáné Földes, Rita/0000-0002-9810-1509}
}

@article{MTMT:1978385,
	title = {Synthesis of ferrocene-labeled steroids via copper-catalyzed azide-alkyne cycloaddition. Reactivity difference between 2β-, 6β- and 16β-azido-androstanes},
	url = {https://m2.mtmt.hu/api/publication/1978385},
	author = {Fehér, Klaudia and Balogh, J and Csók, Zsolt and Kégl, Tamás and Kollár, László and Skodáné Földes, Rita},
	doi = {10.1016/j.steroids.2012.04.005},
	journal-iso = {STEROIDS},
	journal = {STEROIDS},
	volume = {77},
	unique-id = {1978385},
	issn = {0039-128X},
	year = {2012},
	eissn = {1878-5867},
	pages = {738-744},
	orcid-numbers = {Skodáné Földes, Rita/0000-0002-9810-1509}
}