Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Édua Kovács"'
Autor:
Édua Kovács, Hazhmat Ali, Renáta Minorics, Péter Traj, Vivien Resch, Gábor Paragi, Bella Bruszel, István Zupkó, Erzsébet Mernyák
Publikováno v:
Molecules, Vol 28, Iss 3, p 1196 (2023)
Novel 13α-estrone derivatives have been synthesized via direct arylation of the phenolic hydroxy function. Chan–Lam couplings of arylboronic acids with 13α-estrone as a nucleophilic partner were carried out under copper catalysis. The antiprolife
Externí odkaz:
https://doaj.org/article/a3ec26607c184587b7bd532a93501e55
Autor:
Rebeka Jójárt, Péter Traj, Édua Kovács, Ágnes Horváth, Gyula Schneider, Mihály Szécsi, Attila Pál, Gábor Paragi, Erzsébet Mernyák
Publikováno v:
Molecules, Vol 24, Iss 9, p 1783 (2019)
Fluorination of 13-epimeric estrones and their 17-deoxy counterparts was performed with Selectfluor as the reagent. In acetonitrile or trifluoroacetic acid (TFA), 10β-fluoroestra-1,4-dien-3-ones were formed exclusively. Mechanistic investigations su
Externí odkaz:
https://doaj.org/article/87d9d2e1fda9488b82298defd5fa7285
Autor:
Attila Pál, Gyula Schneider, Ágnes Horváth, Erzsébet Mernyák, Gábor Paragi, Rebeka Jójárt, Édua Kovács, Mihály Szécsi, Péter Traj
Publikováno v:
Molecules
Molecules, Vol 24, Iss 9, p 1783 (2019)
Volume 24
Issue 9
Molecules, Vol 24, Iss 9, p 1783 (2019)
Volume 24
Issue 9
Fluorination of 13-epimeric estrones and their 17-deoxy counterparts was performed with Selectfluor as the reagent. In acetonitrile or trifluoroacetic acid (TFA), 10&beta
fluoroestra-1,4-dien-3-ones were formed exclusively. Mechanistic investiga
fluoroestra-1,4-dien-3-ones were formed exclusively. Mechanistic investiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8d3bdfd9885fa32987f357a810f467e
http://europepmc.org/articles/PMC6540200
http://europepmc.org/articles/PMC6540200