Title
Nova biološki aktivna sintetska azaheterociklična jedinjenja i novi sekundarni metaboliti iz odabranih biljnih vrsta: sinteza, izolovanje i spektralna karakterizacija
Creator
Zlatković, Dragan B. 1984-
Copyright date
2018
Object Links
Select license
Autorstvo-Nekomercijalno-Bez prerade 3.0 Srbija (CC BY-NC-ND 3.0)
License description
Dozvoljavate samo preuzimanje i distribuciju dela, ako/dok se pravilno naznačava ime autora, bez ikakvih promena dela i bez prava komercijalnog korišćenja dela. Ova licenca je najstroža CC licenca. Osnovni opis Licence: http://creativecommons.org/licenses/by-nc-nd/3.0/rs/deed.sr_LATN. Sadržaj ugovora u celini: http://creativecommons.org/licenses/by-nc-nd/3.0/rs/legalcode.sr-Latn
Language
Serbian
Cobiss-ID
Theses Type
Doktorska disertacija
description
Datum odbrane: 18.02.2019.
Other responsibilities
mentor
Radulović, Niko 1981-
član komisije
Popsavin, Mirjana 1951-
član komisije
Dekić, Vidoslav
član komisije
Ilić-Tomić, Tatjana
član komisije
Ranđelović, Pavle
Academic Expertise
Prirodno-matematičke nauke
Academic Title
-
University
Univerzitet u Nišu
Faculty
Prirodno-matematički fakultet
Group
Odsek za hemiju
Alternative title
New biologically active synthetic azaheterocyclic compounds and new secondary metabolites from selected plant species: synthesis, isolation and spectral characterization
Publisher
[D. B. Zlatković]
Format
297 str.
description
[O autoru] : Dragan Zlatković: str. [299-301];
Bibligrafija: str. 179-189.
description
Organic chemistry and biochemistry
Abstract (en)
The aim of this PhD thesis was the discovery of new biologically active
compounds either by means of natural product isolation from selected plant
taxa or by organic synthesis. All of the either isolated or synthesized
compounds were characterized by spectroscopic methods, including one- and
two-dimensional NMR experiments. The specific compounds that were the
subject of this research were: aromatic esters from Ferula ovina (Apiaceae),
octyl esters from Heracleum sphondylium (Apiaceae), diesters of an
oxygenated germacrane derivative from Daucus carota (Apiaceae),
isothiocyanates from Reseda lutea (Resedaceae) and germacrone epoxides
from Geranium macrorrhizum (Geraniaceae). Also, as a part of this
dissertation, a synthesis of new ferrocene-indole hybrids and the investigation
of complex metal hydride reduction of Biginelli compounds was performed.
A number of these compounds were tested for their biological activities
(antimicrobial, cytotoxic, antinociceptive and antiacetylcholinesterase
activities).
Authors Key words
Organska sinteza, izolovanje prirodnih proizvoda, spektralna
karakterizacija, feroceni, indoli, Biđinelijeva jedinjenja
Authors Key words
Organic synthesis, natural product isolation, spectral characterization,
ferrocenes, indoles, Biginelli compounds
Classification
54.057:547.753+547.853.5
Subject
615.322:54.061+543.429.23
Subject
P 390, P 004
Type
Tekst
Abstract (en)
The aim of this PhD thesis was the discovery of new biologically active
compounds either by means of natural product isolation from selected plant
taxa or by organic synthesis. All of the either isolated or synthesized
compounds were characterized by spectroscopic methods, including one- and
two-dimensional NMR experiments. The specific compounds that were the
subject of this research were: aromatic esters from Ferula ovina (Apiaceae),
octyl esters from Heracleum sphondylium (Apiaceae), diesters of an
oxygenated germacrane derivative from Daucus carota (Apiaceae),
isothiocyanates from Reseda lutea (Resedaceae) and germacrone epoxides
from Geranium macrorrhizum (Geraniaceae). Also, as a part of this
dissertation, a synthesis of new ferrocene-indole hybrids and the investigation
of complex metal hydride reduction of Biginelli compounds was performed.
A number of these compounds were tested for their biological activities
(antimicrobial, cytotoxic, antinociceptive and antiacetylcholinesterase
activities).
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