Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Vladimir Divjaković"'
Publikováno v:
Journal of the Serbian Chemical Society, Vol 68, Iss 4-5, Pp 425-433 (2003)
The template reaction of a warm methanolic solution of FeCl3.6H2O, S-methylisothiosemicarbazidehydroiodide and 2,6-diacetylpyridine in the presence of LiOAc and NaN3 yielded the high-spin complex [Fe(HL)(N3)2], were HL is the monoanion of the ligand
Externí odkaz:
https://doaj.org/article/0a093a56322e424eba0dcb25daaae903
Autor:
LJILJANA S. VOJINOVIĆ-JEŠIĆ, VUKADIN M. LEOVAC, MIRJANA M. LALOVIĆ, VALERIJA I. ČEŠLJEVIĆ, LJILJANA S. JOVANOVIĆ, MARKO V. RODIĆ, VLADIMIR DIVJAKOVIĆ
Publikováno v:
Journal of the Serbian Chemical Society, Vol 76, Iss 6, Pp 865-877 (2011)
The first two complexes of dioxovanadium(V) with salicylaldehyde thiosemicarbazone (SALTSC), of the coordination formulas [VO2(SALTSC––H)]∙H2O (1) and NH4[VO2(SALTSC–2H] (2), were synthesized and characterized by elemental analysis, conductom
Externí odkaz:
https://doaj.org/article/a7e811b54bb64306836e159ac34f2fb6
Autor:
VUKADIN M. LEOVAC, VLADIMIR DIVJAKOVIĆ, MILAN D. JOKSOVIĆ, LJILJANA S. JOVANOVIĆ, LJILJANA S. VOJINOVIĆ-JEŠIĆ, VALERIJA I. ČEŠLJEVIĆ, MILENA MLINAR
Publikováno v:
Journal of the Serbian Chemical Society, Vol 75, Iss 8, Pp 1063-1074 (2010)
This work is concerned with the synthesis of neutral dioxovana-dium(V) and dioxomolybdenum(VI) complexes with tridentate ONN pyri-doxal S-methylisothiosemicarbazone (PLITSC) of the respective formulas [VO2(PLITSC–H)]•2H2O and [MoO2(PLITSC–2H)].
Externí odkaz:
https://doaj.org/article/b16c5c902b844cdc978d3bdaa6f945bb
Autor:
Sladjana B. Novaković, Dragana Stevanović, Vladimir Divjaković, Goran A. Bogdanović, Rastko D. Vukićević
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 7, Pp m979-m980 (2012)
The title ferrocene-containing Mannich base, [Fe(C5H5)(C16H16NO2)], crystallizes with two independent molecules (A and B) in the asymmetric unit. Molecules A and B have similar conformations. The dihedral angles between the best planes of the benzene
Externí odkaz:
https://doaj.org/article/2ea10c768d8f4027904dd81a074a91c7
Autor:
Sladjana B. Novaković, Mirjana Lalović, Vladimir Divjaković, Ljiljana S. Vojinović-Ješić, Valerija I. Češljević
Publikováno v:
Acta Crystallographica Section E, Vol 66, Iss 8, Pp o1916-o1917 (2010)
The reaction of aqueous solutions of aminoguanidine hydrogennitrate and acetylacetone produces the title pyrazole salt, C7H18N82+·2NO3−. The crystal structure is stabilized by a complex N—H...O hydrogen-bonding network. The difference in the eng
Externí odkaz:
https://doaj.org/article/c7f740f6dc7b45c399528ed3401a4049
Autor:
Marko V. Rodić, Ivana Kovačević, Vladimir Divjaković, Gordana Bogdanović, Tatjana Srdic-Rajic, Dimitar Jakimov, Goran Benedeković, Vesna Kojić, Velimir Popsavin, Mirjana Popsavin
Publikováno v:
European Journal of Medicinal Chemistry. 108:594-604
A new synthesis of goniobutenolides A (1) and B (2) and the corresponding 7-epimers has been achieved starting from diacetone d-glucose. The key step of the synthesis is a new one-pot sequence that commenced with Z-selective Wittig (or Horner-Wadswor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe3c307b1387fbb3db7c253ef8239f63
https://doi.org/10.1016/j.ejmech.2015.12.011
https://doi.org/10.1016/j.ejmech.2015.12.011
Autor:
Velimir Popsavin, Mirjana Popsavin, Gordana Bogdanović, Vladimir Divjaković, Jelena Kesić, Dimitar Jakimov, Ivana Kovačević, Tatjana Srdic-Rajic, Goran Benedeković, Vesna Kojić
Publikováno v:
European journal of medicinal chemistry. 134
Naturally occurring styryl lactone, crassalactone D (1), unnatural 4-epi-crassalactone D (2), and the corresponding 7-epimers (3 and 4) have been synthesized starting from D-glucose. The key step of the synthesis is a new one-pot sequence that commen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::521a852e016a7e0d02991928ce5a0195
https://pubmed.ncbi.nlm.nih.gov/28427016
https://pubmed.ncbi.nlm.nih.gov/28427016
Autor:
Ivana Kovačević, Vladimir Divjaković, Gordana Bogdanović, Mirjana Popsavin, Jovana Francuz, Goran Benedeković, Velimir Popsavin, Vesna Kojić
Publikováno v:
European Journal of Medicinal Chemistry. 87:237-247
A series of styryl lactones containing the cinnamic acid ester groups such as (+)-crassalactones B (3a) and C (4a), 5,7-di-O-cinamoyl derivative 6, the corresponding 7-epimers and 7-deoxy derivatives have been synthesized, characterized and evaluated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef630d6fae0e9aed189fa098a63965fe
https://doi.org/10.1016/j.ejmech.2014.09.064
https://doi.org/10.1016/j.ejmech.2014.09.064
Autor:
Mirjana Popsavin, Gordana Bogdanović, Bojana Srećo Zelenović, Jovana Francuz, Ivana Kovačević, Goran Benedeković, Vladimir Divjaković, Velimir Popsavin, Vesna Kojić
Publikováno v:
European Journal of Medicinal Chemistry. 82:449-458
Synthesis of conformationally restricted (+)-goniofufurone (1) and 7-epi-(+)-goniofufurone (2) analogues, with embedded O-isopropylidene, O-methylidene or cyclic carbonate functions is disclosed starting from d-glucose. A number of potential bioisost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::864d47833097989a03588878f611be52
https://doi.org/10.1016/j.ejmech.2014.05.081
https://doi.org/10.1016/j.ejmech.2014.05.081
Autor:
Dimitar Jakimov, Jovana Francuz, Vesna Kojić, Eva S. Lončar, Lidija D. Aleksić, Tatjana Srdic-Rajic, Vladimir Divjaković, Marko V. Rodić, Gordana Bogdanović, Ivana Kovačević, Mirjana Popsavin, Velimir Popsavin, Bojana Srećo Zelenović, Goran Benedeković
Publikováno v:
European journal of medicinal chemistry. 128
A series of new antitumour lactones containing the [3.3.0] bicyclic furano-lactone core and the halogen or azido group at the C-7 position have been designed, synthesized, and evaluated for their in vitro antitumour activity against a panel of human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb530f0bd6202f87ef80e97ac6c957cd
https://pubmed.ncbi.nlm.nih.gov/28135634
https://pubmed.ncbi.nlm.nih.gov/28135634