
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/">
  <dc:creator>Mladenović, Marko Z. 1987-</dc:creator>
  <dc:identifier>https://phaidrani.ni.ac.rs/o:1372</dc:identifier>
  <dc:identifier>cobiss:1025474025</dc:identifier>
  <dc:identifier>thesis:5126</dc:identifier>
  <dc:description xml:lang="eng">Herein, a successful identification and a means of arriving at (milli)gram quantities of the selected
natural esters was achieved through the application of a synthetic combinatorial approach (three
libraries with 171 constituents in total, among them 121 new compounds). As a result, new secondary
metabolites from Achillea falcata L. ((1R*,3S*,5R*)-sabinyl formate and tiglate), Achillea ageratifolia
(Sm.) Boiss. subsp. serbica (Nyman) Heimerl ((1R*,3S*,5R*)-sabinyl formate, tiglate, nonanoate and
decanoate), Scandix balansae Reut. ex Boiss. (octadecyl valerate), Scandix pecten-veneris L. (esters of
isobutanoic acid and n-C15, C17, C21 and C23 alkanols, as well as esters of isovaleric acid and n-C13, C15
and C17 alkanols) and Anthemis segetalis Ten. (eugenyl angelate, 2-methylbutanoate and 3-
methylbutanoate) essential-oil samples wеre identified. Also, the combinatorial approach was successful
used for a systematical comparison of chemical/biological properties of ferrocene-containing esters and
their corresponding phenyl analogs (a library of eighteen (13 new) 2-substituted methyl acetoacetates).
The structures of the synthesized esters were spectrally characterized by MS, NMR (1D- and 2D-NMR,
as well as, an NMR methodology that employ lanthanide-induced shifts), FTIR and UV-Vis analyses,
and in the case of ferrocene-containing compounds by electrochemical (cyclic voltammetry) and X-ray
analyse(s). Several esters were shown to be toxic to A. salina, possessed cytotoxic (to two cell lines),
AChE inhibitory, antinociceptive and antimicrobial activities. Antinociceptive activity of
(1R*,3S*,5R*)-sabinol was two times higher than that of morphine, and the antifungal activity of 2-
acetyl-2-(ferrocenylmethyl)-4-methyl-4-pentenoate was comparable to that of nystatin against Candida
albicans.</dc:description>
  <dc:description xml:lang="srp"></dc:description>
  <dc:type>info:eu-repo/semantics/bachelorThesis</dc:type>
  <dc:rights>http://creativecommons.org/licenses/by-nc-nd/2.0/at/legalcode</dc:rights>
  <dc:date>2017</dc:date>
  <dc:contributor>Radulović, Niko 1981-</dc:contributor>
  <dc:contributor>Blagojević, Polina 1979-</dc:contributor>
  <dc:contributor>Novaković, Irena</dc:contributor>
  <dc:contributor>Todorović, Tamara</dc:contributor>
  <dc:contributor>Stojanović-Radić, Zorica</dc:contributor>
  <dc:title xml:lang="srp">Kombinatorne biblioteke odabranih prirodnih i sintetskih biološki aktivnih estara</dc:title>
  <dc:format>554 listova</dc:format>
  <dc:format>68861019 bytes</dc:format>
  <dc:language>srp</dc:language>
</oai_dc:dc>
