Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Tatjana Kop"'
Publikováno v:
Journal of the Serbian Chemical Society, Vol 69, Iss 10, Pp 769-775 (2004)
Synthesis of a steroidal dendrimer core possessing various functional termini, such as ester, carboxy and hydroxy, is presented. The approach described enables further simple manipulations for the introduction of more complex functionalities.
Externí odkaz:
https://doaj.org/article/f48ce7fcf38c4daba9e7f0e8ebffe07f
Effects of fullerene C60 supplementation on gut microbiota and glucose and lipid homeostasis in rats
Autor:
Snežana Pejić, Tatjana Kop, Nebojša Jasnić, Gorana Nikolić, Dragana Milić, Zoran Todorovic, Vesna Martinović, Jelena Đorđević, Dragana Mitić-Ćulafić, Ana Todorović, Siniša Đurašević, Dunja Drakulić
Publikováno v:
Food and Chemical Toxicology
The effects of twelve weeks of supplementation with fullerene C60 olive/coconut oil solution on a broad spectrum of parameters in rats were examined. The tissue bioaccumulation of C60 was shown to be tissue-specific, with the liver, heart, and adrena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8899a0337dd2e15b78522f77448b4b0f
https://cherry.chem.bg.ac.rs/handle/123456789/3994
https://cherry.chem.bg.ac.rs/handle/123456789/3994
Autor:
Mira S. Bjelaković, Vladimir Beškoski, Tatjana Kop, Dragica Jakovljević, Dragana Milić, Gordana Gojgić-Cvijović, Ljiljana Živković, Andrijana A. Žekić
Publikováno v:
European Polymer Journal
An efficient encapsulation of the fullerene into two hydrophobized and one native polysaccharide provided water soluble supramolecular hybrids. After covalent modification of polysaccharides by cholesterol, noncovalent hybrids were prepared by a thre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01909bbbec6c0aaa2b8d76ade1c720ea
http://cherry.chem.bg.ac.rs/handle/123456789/3765
http://cherry.chem.bg.ac.rs/handle/123456789/3765
Autor:
Manuel Algarra, Lan Mi, Maja Nešić, Tatjana Kop, Jelena Žakula, Aleksandra Mitrovic, Marijana Petković, Milutin Stepić, Mira S. Bjelaković, Lela Korićanac, Gordana D. Gojgić Cvijović, Tanja Dučić, Xinyue Liang
Publikováno v:
International Journal of Biological Macromolecules
Objects of the present study are improved fullerene C60 drug carrier properties trough encapsulation by microbial polysaccharides, levan (LEV), pullulan (PUL), and their hydrophobized cholesterol-derivatives (CHL and CHP), that show better interactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4170198787451f538b73ffd1279e5a75
https://cer.ihtm.bg.ac.rs/handle/123456789/3891
https://cer.ihtm.bg.ac.rs/handle/123456789/3891
Publikováno v:
Beilstein Journal of Nanotechnology, Vol 6, Iss 1, Pp 1065-1071 (2015)
Beilstein Journal of Nanotechnology
Beilstein Journal of Nanotechnology
The potential use of amphiphilic fullerene derivatives as a bionanomaterial was investigated by cyclic voltammetry (CV), scanning electron microscopy (SEM), and the ferrous ion oxidation-xylenol orange (FOX) method. Despite the disrupted delocalizati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18fa590e2983a44f55415a611ceb96f0
https://doaj.org/article/65bfc47e674b494096e58f1d016acf97
https://doaj.org/article/65bfc47e674b494096e58f1d016acf97
Publikováno v:
Tetrahedron
Four macrocyclic bis(pyrrolidino)fullerene regioisomers with e-edge, e-face, trans-4 and cis-2 addition patterns were synthesized from the corresponding monoadduct by Prato's cycloaddition in a yield of 50%, and fully characterized by spectroscopic t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f392ddefdf81ec209b487ac0ec5215f
https://cer.ihtm.bg.ac.rs/handle/123456789/2124
https://cer.ihtm.bg.ac.rs/handle/123456789/2124
Publikováno v:
Journal of Materials Science
A series of N-substituted fulleropyrrolidines containing peptide side chain was synthesized by the quantitative, TFA-mediated deprotection of the corresponding tert-butyl esters. The structures of all compounds were determined by comparative analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0695c8b0d3ac76051f3bd7a2042acc7b
https://cherry.chem.bg.ac.rs/handle/123456789/1999
https://cherry.chem.bg.ac.rs/handle/123456789/1999
Publikováno v:
RSC Advances
Two different alpha,omega-diglicynes linked by linear polyoxaalkyl chains in the presence of formaldehyde underwent Prato reaction to the fullerene C-60. The shorter linker templated formation of only cis-bisadducts, while the longer one afforded a m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b47ebe00fd4ae6703e089bc5b3908c1
https://cer.ihtm.bg.ac.rs/handle/123456789/1829
https://cer.ihtm.bg.ac.rs/handle/123456789/1829
Publikováno v:
Tetrahedron
The one-pot bistycloaddition of alkyl-tethered diglycines to C-60 provided five series of bridged bis(pyrrolidino)fullerenes with good regioselectivity, giving mainly cis-2 and cis-3 products. An influence of the bridge length and addition pattern on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab6d80971387076043670c512d56b38b
https://cherry.chem.bg.ac.rs/handle/123456789/1729
https://cherry.chem.bg.ac.rs/handle/123456789/1729
Autor:
Tatjana Kop, Miroslav J. Gašić, Dragana Milić, Gabriella Pocsfalvi, Zorica Juranić, Bernard Tinant, Bogdan A. Šolaja
Publikováno v:
Steroids
A simple approach to aromatization of steroidal quinols and epoxyquinols using a catalytic amount of TMSOTf is reported. Beside acetylation of the angular OH, the acid-catalyzed (TfOH) dienone-phenol rearrangement occurred affording "para" products,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8502b158cdbe1f3b267eb6474a827023
https://doi.org/10.1016/j.steroids.2005.07.001
https://doi.org/10.1016/j.steroids.2005.07.001