
<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:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/at/legalcode</dc:rights>
  <dc:description xml:lang="srp">This doctoral dissertation presents the chemical composition of thewashings of Primula veris L., Primula acaulis (L.) L. andLiriodendron tulipifera L. The studied Primula species were rich inlong-chain branched alkanes. For the first time, 19 new long-chain n-,iso-, and anteiso-benzyl alkanoates, as well as 8 iso- and 6 anteiso-2-alkanones were identified in samples of natural origin. Evennumberediso-alkanes and 2-alkanones, and iso-odd-numbered fattyacid benzyl esters, are unique for Primula spp. Washings of P. veriscontained new: 16 syn-1-phenylalkane-1,3-diyl diacetates, 7 3-oxo-1-phenylalkan-1-yl acetates, 8 1-phenylalkane-1,3-diones, and 10 1-Hydroxy-1-phenylalkan-3-ones, with n-, iso- and anteiso-chaintermini.Also, 79 n-, iso-, and anteiso-sec-alcohols were identified (66new), and 77 long-chain n-, iso-, anteiso-, 2-methyl-, and 3-methylfatty acids. All long-chain 2-methyl- and 3-methyl acids werefound in the Plant Kingdom for the first time. Benzyl esters lower thewax melting point, which increases the permeability of the cuticle,and reduce the harmful effects of UV-C radiation. Washings of L.tulipifera flowers, among the most abundant palmitone, contained nalkanes,(E)-n-alkenes, regioisomeric alk(en)als, alkanones, and (Z)-alk(en)-1-ols. Double bond regiochemistry was inferred from DMDSadducts MS. Where possible, the configuration was inferred from theNMR analysis of cyclopropanation adducts. 10/11-Hydroxy-16-hentriacontanones were identified based on the analysis oftrimethylsilyl derivatives of hydroxy-ketone and bis(trimethylsilyl)derivatives of hentriacontanediols MSes. GC-MS analysis of L.tulipifera leaf washings samples revealed that the main constituentwas palmitone, while separate GC-MS analyses of petals, sepals, andpistils with anthers, revealed palmitone to be predominant on thepetal and sepal surfaces.</dc:description>
  <dc:description xml:lang="srp">Bibligrafija: str. 179-189.  Datum odbrane: 26.08.2022. Organic chemistry and biochemistry, organic synthesis</dc:description>
  <dc:type>info:eu-repo/semantics/bachelorThesis</dc:type>
  <dc:identifier>https://phaidrani.ni.ac.rs/o:1845</dc:identifier>
  <dc:identifier>cobiss:73701897</dc:identifier>
  <dc:identifier>thesis:8570</dc:identifier>
  <dc:creator id="https://plus.cobiss.net/cobiss/sr/sr/conor/89372425">Živković Stošić, Milena, 1987-</dc:creator>
  <dc:language>srp</dc:language>
  <dc:format>320 str.</dc:format>
  <dc:format>12381681 bytes</dc:format>
  <dc:title xml:lang="srp">Identifikacija i sinteza odabranih sastojaka voskova biljnih vrsta Prima veris L., Primula acaulis(L.) L. (Primulaceae) I Liriodendron tulipifera L. (Magnoliaceae)</dc:title>
  <dc:contributor id="https://plus.cobiss.net/cobiss/sr/sr/conor/8429415">Radulović, Niko, 1981-</dc:contributor>
  <dc:contributor id="https://plus.cobiss.net/cobiss/sr/sr/conor/9679719">Stojanović, Gordana, 1960-</dc:contributor>
  <dc:contributor id="https://plus.cobiss.net/cobiss/sr/sr/conor/11173991">Zlatković, Bojan, 1970-</dc:contributor>
  <dc:contributor id="https://plus.cobiss.net/cobiss/sr/sr/conor/72061961">Genčić, Marija S., 1985-</dc:contributor>
  <dc:contributor id="https://plus.cobiss.net/cobiss/sr/sr/conor/69160201">Dekić, Milan S., 1980-</dc:contributor>
  <dc:date>2022</dc:date>
</oai_dc:dc>
