Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ljubica Grbović"'
Autor:
Ksenija Pavlović, Ljubica Grbović, Milica Karadžić Banjac, Strahinja Kovačević, Anamarija Mandić, Sanja Podunavac-Kuzmanović, Bojana Vasiljević
Publikováno v:
Macedonian Journal of Chemistry and Chemical Engineering, Vol 42, Iss 2 (2023)
In this study, eco-friendly microwave-assisted esterification reactions of chenodeoxycholic acid with medium-chain diols (1,2-ethanediol, 1,4-butanediol, 1,6-hexanediol, 1,8-octanediol, and 1,10-decanediol) or tetraethylene glycol were accomplished.
Externí odkaz:
https://doaj.org/article/882b9a27da694b0fb720805716679f0b
Autor:
Ljubica Grbović, Bojana Radovan Vasiljević, Ksenija Pavlović, Timea Hajnal-Jafari, Simonida Đurić, Mirjana Popsavin, Slavko Kevrešan
Publikováno v:
Macedonian Journal of Chemistry and Chemical Engineering, Vol 37, Iss 1, Pp 13-20 (2018)
Within the field of green chemistry, a noticeable results were obtained in the solvent-free synthesis of amide derivatives of naphthenic acids under microwave irradiation. Naphthenic acid amides, anilides, and morpholides were synthesized directly fr
Externí odkaz:
https://doaj.org/article/0dbcf19cd0294398abfbf27d269fb44e
Publikováno v:
Journal of Surfactants and Detergents. 18(1):83-89
The aim of this study was to investigate micellar and self-assembly properties of four sodium salts of naphthenic acid mixtures by determination and comparative analysis of their critical micelle concentration values at seven different temperatures r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d81d09f8c16097511097157f14c4841
https://doi.org/10.1007/s11743-014-1596-z
https://doi.org/10.1007/s11743-014-1596-z
Autor:
Marko Ilić, Kristian Pastor, Jelena Marković, Ljubica Grbović, Suzana Jovanović-Šanta, Ivana Mitrović, Zorana Trivunović, Marijana Ačanski
Publikováno v:
Steroids. 186
Organic synthesis could be very demanding, usually due to difficulties related to the separation of main reaction products from by-products. Steroidal compounds could have similar lipophilicity, which is mostly based on the lipophilicity of the stero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45d67487fd59b96e50bb2e65edc376d2
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85133531048&doi=10.1016/j.steroids.2022.109074&partnerID=40&md5=a659403136247e6fa889f25919be1bf2
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85133531048&doi=10.1016/j.steroids.2022.109074&partnerID=40&md5=a659403136247e6fa889f25919be1bf2
Publikováno v:
Current Organic Chemistry. 23(3):256-275
The first attempts at microwave-assisted (MW) syntheses of bile acid derivatives were performed in domestic MW appliances. However, the reproducibility of these syntheses, which were performed in uncontrolled conditions, was very low. In the first pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fb161939a35cbad10a53fb97feb02fb
https://doi.org/10.2174/1385272823666190213114104
https://doi.org/10.2174/1385272823666190213114104
Publikováno v:
JPC - Journal of Planar Chromatography - Modern TLC. 31:497-504
It has been established that the selected acetamide derivatives fulfill Veber's and Pardridge's rule of good bioavailability. The lipophilicity as a crucial molecular descriptor of biological activity for acetamide derivatives was determined by rever
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ef369d559b29512e623d338308b1450
https://doi.org/10.1556/1006.2018.31.6.10
https://doi.org/10.1556/1006.2018.31.6.10
Publikováno v:
Journal of Physical Organic Chemistry. 34(2)
Bile acid salts are amphiphiles that have planar polarity: the convex surface (the β side) of their steroid skeleton is hydrophobic, whereas the concave surface (the α side) is hydrophilic. Lactone and lactam derivatives of bile acid salts have red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c759a73c11cd81dd617bcf5ab145ea2f
https://www.cris.uns.ac.rs/record.jsf?recordId=116018&source=OpenAIRE&language=en
https://www.cris.uns.ac.rs/record.jsf?recordId=116018&source=OpenAIRE&language=en
Autor:
Sofija S. Bekić, Edward T. Petri, Ljubica Grbović, Bojana Vasiljević, Ksenija Pavlović, Andjelka S. Ćelić
Publikováno v:
RSC Med Chem
Herein, we present microwave-assisted AlCl(3) catalyzed oxidation of bile acid hydroxyl groups in the presence of Oxone® in water media. Significant rate enhancements were observed for Wolff–Kishner reduction of synthesized bile acids oxo derivati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a85a3e00ad02ce6fce7b363177eb7257
https://pubmed.ncbi.nlm.nih.gov/34046616
https://pubmed.ncbi.nlm.nih.gov/34046616
Autor:
Timea Hajnal-Jafari, Simonida Đurić, Ljubica Grbović, Mirjana Popsavin, Slavko Kevrešan, Bojana Vasiljević, Ksenija Pavlović
Publikováno v:
Macedonian Journal of Chemistry and Chemical Engineering, Vol 37, Iss 1, Pp 13-20 (2018)
Within the field of green chemistry, a noticeable results were obtained in the solvent-free synthesis of amide derivatives of naphthenic acids under microwave irradiation. Naphthenic acid amides, anilides, and morpholides were synthesized directly fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c085db55d60c5d3fc53c6a06e60e730
https://mjcce.org.mk/index.php/MJCCE/article/view/1371
https://mjcce.org.mk/index.php/MJCCE/article/view/1371
Autor:
Slobodan Gadžurić, Sanja Belić, Sanja O. Podunavac-Kuzmanović, Nebojša Zec, Milan Vraneš, Strahinja Z. Kovačević, Ljubica Grbović
Publikováno v:
Journal of Molecular Liquids. 229:212-216
Physicochemical properties and nature of the interactions in methanol and ethanol solutions of 1-butyl-3-ethylimidazolium bromide ionic liquid, [C4C2im]Br, have been investigated experimentally measuring density over the whole composition range at se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ad6539808399babe56a13c3044f8562
https://doi.org/10.1016/j.molliq.2016.12.052
https://doi.org/10.1016/j.molliq.2016.12.052