Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Silvio Jakopec"'
Autor:
Silvija Maračić, Silvio Jakopec, Martina Piškor, Marijana Leventić, Jasmina Lapić, Senka Djaković, Mario Cetina, Ljubica Glavaš‐Obrovac, Silvana Raić‐Malić
Publikováno v:
Applied Organometallic Chemistry.
The synthesis of novel 1, 1′-disubstituted ferrocene conjugates appended with N-1 and O-4 alkylated quinolone and quinoline was reported. The target compounds were synthesized employing a liquid-assisted grinding (LAG) mechanochemical method in cop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33bf04ae9733bee9eedd11af037a3c13
https://doi.org/10.1002/aoc.7124
https://doi.org/10.1002/aoc.7124
Autor:
Andrea Bistrović, Popov, Andrijana Meščić, Macan, Silvio, Jakopec, Helena, Prpić, Anja Harej, Hrkać, Sandra Kraljević, Pavelić, Silvana, Raić-Malić
Publikováno v:
Future medicinal chemistry. 14(16)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7b545675fe14d9a358c15e4d82496b59
https://pubmed.ncbi.nlm.nih.gov/35791783
https://pubmed.ncbi.nlm.nih.gov/35791783
Autor:
Dijana Jadreško, Anamaria Brozovic, Berislav Peric, Srecko Kirin, Natalija Pantalon Juraj, Silvana Raić-Malić, Silvio Jakopec
Publikováno v:
Applied Organometallic Chemistry. 36
Ferrocene derivatives with mono- (8a–c) and bis- 1, 2, 3-triazolyl (9 and 10a–13c) chelating groups were synthesized by regioselective copper(I)- catalysed 1, 3-dipolar cycloaddition of terminal alkynes with ferrocene azides. Metal complexes of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a59db889b73c46ae7106a3e714d60f05
https://doi.org/10.1002/aoc.6575
https://doi.org/10.1002/aoc.6575
Autor:
Andrea Bistrović Popov, Andrijana Meščić Macan, Silvio Jakopec, Helena Prpić, Anja Harej Hrkać, Sandra Kraljević Pavelić, Silvana Raić-Malić
Aim: The authors' aim was to improve the application of copper-catalyzed azide-alkyne cycloaddition in the synthesis of hybrids containing biologically significant nucleobases and L-ascorbic acid scaffolds by introducing an environmentally friendly a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e26b347c9efb9f3cc761c6328d96fd85
https://doi.org/10.4155/fmc-2022-0047
https://doi.org/10.4155/fmc-2022-0047
Autor:
Nataša Perin, Marijana Radić Stojković, Marija Mioč, Marijeta Kralj, Silvio Jakopec, Andrijana Meščić Macan, Silvana Raić-Malić, Marijana Hranjec
Publikováno v:
European journal of medicinal chemistry. 185
The three series of 5-mono- and 2,5-bis-1,2,3-triazolyl-substituted benzimidazo[1,2-a]quinolines as potential antitumor agents were synthesized. Their growth-inhibitory activity is influenced by the introduction of fluorine at C-2 and the mono-triazo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::867e92e63ba2c43db4792ad47a98faac
https://pubmed.ncbi.nlm.nih.gov/31718941
https://pubmed.ncbi.nlm.nih.gov/31718941