Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Krešimir Sanković"'
Autor:
Valerije Vrček, Valentina Havaić, Senka Djaković, Jasmina Lapić, Krešimir Sanković, Davor Šakić
Publikováno v:
European Journal of Organic Chemistry. 2015:5424-5431
Uracil, thymine, and 5-fluorouracil (5-FU) have been ferrocenoylated selectively at the N1 position. Deprotonated pyrimidine nucleobases, prepared with sodium hydride (NaH) in N,N-dimethylformamide (DMF), reacted with either ferrocenoyl chloride (FcC
Publikováno v:
Acta Crystallographica Section C: Crystal Structure Communications
The crystallization and characterization of a new polymorph of 2-thiouracil by single-crystal X-ray diffraction, Hirshfeld surface analysis and periodic density functional theory (DFT) calculations are described. The previously published polymorph (A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1646543ded584111db09910f5ece27b
https://doi.org/10.1107/s205322961701542x
https://doi.org/10.1107/s205322961701542x
Autor:
Irena Ivanišević, Vlasta Mohaček-Grošev, Viktor Pilepić, Ivana Fabijanić, Krešimir Sanković, Dubravka Matković-Čalogović
Crystals of the guanine trichloro cuprate( II ) complex, (HGua)2[Cu2Cl6]·2H2O (HGua = protonated guanine), were prepared and analysed by spectroscopic (IR, Raman) and computational methods. A new single-crystal X-ray diffraction analysis was conduct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::643517d5c934705e7123e7ebc3c3092c
https://doi.org/10.1016/j.molstruc.2016.08.069
https://doi.org/10.1016/j.molstruc.2016.08.069
Autor:
Ksenija Karlović, Marijana Zovko, Ivan Kosalec, Dario Kremer, Barbara Gregurek, Krešimir Sanković
Publikováno v:
World Journal of Microbiology and Biotechnology. 25:145-150
By using HPLC/UV– VIS, Croatian barberry (Berberis croatica Horvat) was found to be a new source of the bioactive alkaloid berberine. Comparison of berberine content in roots, leaves, and twigs between wild specimens of B. croatica and B. vulgaris
Publikováno v:
European Journal of Medicinal Chemistry. 40:51-55
Redox behaviour of the iron(III) complex with the antitumour drug hydroxyurea was studied by cyclic voltammetry. The complex underwent a one-electron reduction, followed by an irreversible chemical reaction (EC mechanism) in which a ligand was releas
Publikováno v:
Zeitschrift f�r anorganische und allgemeine Chemie. 630:2749-2753
Products and reaction stoichiometry of the interaction between iron(III) and hydroxyurea (HU) in aqueous solutions were studied. Under condition of an excess of iron(111) over hydroxyurea, initially formed mono(hydroxyurea)iron(III) complex decompose
Publikováno v:
Physical Chemistry Chemical Physics. 2:4971-4975
ENDOR spectroscopy was used for the analysis of radiation-induced electron-loss radicals in thiocytosine. The radicals were induced by X-irradiating single crystals of cytosine monohydrate, substitutionally doped with 2-thiocytosine. X-irradiation an
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 61:o3846-o3848
The structure of the title compound (systematic name: 6-amino-2-thioxo-2,3-dihydropyrimidin-1-ium bromide), C4H6N3S+·Br−, has two 2-thiocytosinium cations and two Br− anions in the asymmetric unit and is isostructural with 2-thiocytosinium
Publikováno v:
International Journal of Radiation Biology. 70:603-608
It has been demonstrated that the paramagnetic species formed in crystals of cytosine hydrochloride doped with thiocytosine are most likely the radicals formed by association of thiocytosine and chlorine. The unpaired electron is positively identifie
Publikováno v:
Physical Chemistry Chemical Physics. 3:2723-2725
Thioanalogs of the nucleic-acid bases are known photosensitive probes and good traps of radiation energy. Radiation-induced sulfur-centered free radicals stabilized on the base thioanalogs molecules are of the cationic origin. Their electronic config