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Akademický článek
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Autor:
Beriša, Arben, Gredičak, Matija
Stereoselective arylation of diaryl ketimines to afford products containing quaternary stereogenic centers bearing three aryl groups is challenging because of the steric hindrance on such stereocenters. The problem lies in the inherent difficulty for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::8f44b382ac21a3d9710a565ed99199d7
https://www.bib.irb.hr/1217275
https://www.bib.irb.hr/1217275
Autor:
Beriša, Arben
U sklopu ove doktorske radnje razvijen je protokol koji opisuje sintezu derivata izoindolinona s triaril-supstituiranim kvaternim stereogenim centrom u organokatalitičkim uvjetima. Provedeno je stereoselektivno i regioselektivno ariliranje izoindoli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6559b7aadc4dbbc32b6fc7783c5fdbe4
https://www.bib.irb.hr/1240117
https://www.bib.irb.hr/1240117
Autor:
Beriša, Arben, Gredičak, Matija
Enantiomerically pure 3, 3-disubstituted isoindolinones are represented as highly valuable structural motifs found in a numerous of natural products and biologically active compounds. Their biological activities are greatly influenced by the type of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::481610309c8b606c78a52afa7946a27c
https://www.bib.irb.hr/1191249
https://www.bib.irb.hr/1191249
Autor:
Beriša, Arben, Gredičak, Matija
Stereoselective functionalization of pyrroles is a challenging task. Because of their inherent small molecular size, the coordination of pyrroles with chiral catalysts results in weak steric interactions, which leads to difficulties in controlling th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::67bea3eee7876f7f7a75e01adaa2b28f
https://www.bib.irb.hr/1238857
https://www.bib.irb.hr/1238857
Akademický článek
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Autor:
Beriša, Arben, Gredičak, Matija
An enantioselective arlyation of diaryl ketimines with phenols is reported. The generation of new tetrasubstituted stereogenic center comprising two or more aryl substituents in an enantioselective fashion is a challenging task. The problem lies in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::76f6842185246879375e1f2248add59d
https://www.bib.irb.hr/1142726
https://www.bib.irb.hr/1142726
Autor:
Beriša, Arben, Gredičak, Matija
Chiral α-quaternary methanamines are common structural motifs found in a variety of natural products exhibiting wide spectrum of biological activities. Synthesis of such compounds has always been challenging because of the steric hindrance positione
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::4d2a0091455a3f1017b7565d745a575c
https://www.bib.irb.hr/1132916
https://www.bib.irb.hr/1132916
Autor:
Beriša, Arben, Gredičak, Matija
A stereoselective synthesis of α- triarylmethanamine structural motifs via formal Betti reaction is described. Chiral α- triarylmethanamines are represented as ubiquitous building blocks found in a variety of natural products and biologically activ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::d9f4ad823dfb4aaa589c874b40e73a1f
https://www.bib.irb.hr/1126180
https://www.bib.irb.hr/1126180
SYNTHESIS OF NEW NUCLEOS(T)IDE ANALOGUES AND EVALUATION OF THEIR CHOLINESTERASE INIBITORY ACTIVITIES
Autor:
De Sousa, Eduardo, Pereira, Margarida, Beriša, Arben, Pereira, Rita, Loesche, Anne, Csuk, René, Xavier, Nuno
Nucleosides and nucleotides are essential biomolecules in multiple biological processes, such as the synthesis of nucleic acids, cell cycle or cell signaling. These events are essential in health and also for the progress of diseases, such as cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::e02b6e0304ce707a3cc8f68fc519a872
https://www.bib.irb.hr/1067729
https://www.bib.irb.hr/1067729