Mojca Čakić Semenčić
University of Zagreb
17 Papers
114 Citations
Mojca Čakić Semenčić is an academic researcher from University of Zagreb. The author has contributed to research in topics: Ferrocene & Hydrogen bond. The author has an hindex of 6, co-authored 16 publications. Previous affiliations of Mojca Čakić Semenčić include University of Mainz & Heidelberg University.
Chat about Author
Papers
Spectroscopic and Theoretical Study of Asymmetric 1,1′-Diaminoferrocene Conjugates of α-Amino Acids
TL;DR: In this article, the synthesis and characterization of asymmetric 1,1′-diaminoferrocene conjugates of α-amino acids Boc-AA-NHN-Fn-NH-Ac [AA = Gly (10), Ala (11), d-Ala (12), Val (13), Fn = 1, 1′-ferrocenediyl] is reported.
36
Ferrocene-dipeptide conjugates derived from aminoferrocene and 1-acetyl-1′-aminoferrocene: synthesis and conformational studies
TL;DR: In this paper, the synthesis and conformational analysis of mono-and disubstituted ferrocene bioconjugates bearing dipeptide chains (Boc-AA,AA-AA-Fn-X, AA=Gly, l-Ala, L-Val) were presented.
23
The first ferrocene analogues of muramyldipeptide.
Lidija Barišić,Maja Roščić,Monika Kovačević,Mojca Čakić Semenčić,Štefica Horvat,Vladimir Rapić +5 more
TL;DR: The two structurally interesting bioorganometallic analogues of muramyldipeptide (MDP) with potential immunomodulatory activity were synthesized starting from the O-protected N-acetylmuramic acid (MurNAc), L- or D-Ala and 1'-aminoferrocene-1-carboxylic acid (Fca).
20
Synthesis and Conformational Study of Monosubstituted Aminoferrocene‐Based Peptides Bearing Homo‐ and Heterochiral Pro‐Ala Sequences
TL;DR: In this article, the synthesis and conformational analysis of a series of monosubstituted aminoferrocene-based peptides bearing homo- and heterochiral Pro-Ala sequences are described.
12
Tight turn in dipeptide bridged ferrocenes: Synthesis, X-ray structural, theoretical and spectroscopic studies
TL;DR: In this article, a small homochiral sequence of two aminoacids (FcCO-Pro-Ala-NHFc) was prepared using stepwise solution-phase coupling techniques and the propensity of these bioorganometallics to form tight turns that resemble those in natural peptides was investigated by means of spectroscopy and the crystal structure was determined by X-ray diffraction analysis.
11