TY  - JOUR
AU  - Herman, Bianka Edina
AU  - Gardi, János
AU  - Julesz, János
AU  - Tömböly, Csaba
AU  - Szánti-Pintér, Eszter
AU  - Fehér, Klaudia
AU  - Skodáné Földes, Rita
AU  - Szécsi, Mihály
TI  - Steroidal ferrocenes as potential enzyme inhibitors of the estrogen biosynthesis
JF  - BIOLOGIA FUTURA
J2  - BIOL FUTURA
VL  - 71
PY  - 2020
IS  - 3
SP  - 249
EP  - 264
PG  - 16
SN  - 2676-8615
DO  - 10.1007/s42977-020-00023-7
UR  - https://m2.mtmt.hu/api/publication/31365295
ID  - 31365295
LA  - English
DB  - MTMT
ER  - 

TY  - THES
AU  - Fehér, Klaudia
TI  - Rézkatalizált azid-alkin cikloaddíció: szintézis és katalizátorfejlesztés
PB  - Pannon Egyetem
PY  - 2018
SP  - 129
DO  - 10.18136/PE.2018.692
UR  - https://m2.mtmt.hu/api/publication/30982307
ID  - 30982307
LA  - Hungarian
DB  - MTMT
ER  - 

TY  - THES
AU  - Fehér, Klaudia
TI  - Réz-katalizált azid-alkin cikloaddíció: szintézis és katalizátorfejlesztés
PY  - 2018
UR  - https://m2.mtmt.hu/api/publication/30982300
ID  - 30982300
LA  - Hungarian
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Fehér, Klaudia
AU  - Nagy, Enikő
AU  - Szabo, P
AU  - Yuzhakova, Tatiana
AU  - Srankó, Dávid Ferenc
AU  - Gömöry, Ágnes
AU  - Kollár, László
AU  - Skodáné Földes, Rita
TI  - Heterogeneous azide-alkyne cycloaddition in the presence of a copper catalyst supported on an ionic liquid polymer/silica hybrid material
JF  - APPLIED ORGANOMETALLIC CHEMISTRY
J2  - APPL ORGANOMET CHEM
VL  - 32
PY  - 2018
IS  - 6
PG  - 13
SN  - 0268-2605
DO  - 10.1002/aoc.4343
UR  - https://m2.mtmt.hu/api/publication/3400511
ID  - 3400511
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Fehér, Klaudia
AU  - Gömöry, Ágnes
AU  - Skodáné Földes, Rita
TI  - A modular synthesis of 1,4,5-trisubstituted 1,2,3-triazoles with ferrocene moieties
JF  - MONATSHEFTE FUR CHEMIE
J2  - MONATSH CHEM
VL  - 146
PY  - 2015
IS  - 9
SP  - 1455
EP  - 1463
PG  - 9
SN  - 0026-9247
DO  - 10.1007/s00706-015-1490-z
UR  - https://m2.mtmt.hu/api/publication/2940107
ID  - 2940107
AB  - 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.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Fehér, Klaudia
AU  - Balogh, J
AU  - Csók, Zsolt
AU  - Kégl, Tamás
AU  - Kollár, László
AU  - Skodáné Földes, Rita
TI  - Synthesis of ferrocene-labeled steroids via copper-catalyzed azide-alkyne cycloaddition. Reactivity difference between 2β-, 6β- and 16β-azido-androstanes
JF  - STEROIDS
J2  - STEROIDS
VL  - 77
PY  - 2012
IS  - 7
SP  - 738
EP  - 744
PG  - 7
SN  - 0039-128X
DO  - 10.1016/j.steroids.2012.04.005
UR  - https://m2.mtmt.hu/api/publication/1978385
ID  - 1978385
LA  - English
DB  - MTMT
ER  -