Scientific Associate
Address:
ICTM, Center for chemistry, Studentski trg 12-16, 11000 Belgrade, Serbia
Laboratory for Organic Chemistry
Phone : +38111/3336-740
Fax : +38111/2636-061
E-mail : jovanat@chem.bg.ac.rs
Education:
2005. Dipl. chem., Faculty of Chemistry, University of Belgrade
2008. M.Sc, Faculty of Chemistry, University of Belgrade
2013. Ph.D, Faculty of Chemistry, University of Belgrade
2009. Research Assistant
2014. Scientific Associate Societies: Serbian Chemical Society Professional experience: Since 2006. ICTM – Center for chemistry Field of interest: Organic Chemistry, Organic Synthesis, Chemistry of Heterocyclic compounds Languages: english, german (basic) Projects:
International:
2010. - 2011. - DAAD-Project ID 504252270, which was implemented between the group of Professor Rade Markovic, Faculty of Chemistry, University of Belgrade and Professor Erik Kleinpeter, the Institute of Chemistry of the University of Potsdam, Germany
1. 10. 2009. - 31. 03. 2010. - Guest student in research group of Prof. Peter Langer in Institute of Chemistry, Rostock, Germany
National:
2006. - 2010. - Thiazolidines and synthetic analogues: reactivity, application and biological activity, project number 142007, under the direction of Dr. Rade Markovic, professor of the Faculty of Chemistry , University of Belgrade
2011. - .... - Experimental and theoretical study of reactivity and biological activity stereodefined thiazolidines and synthetic analogues , project number 172020 , under the direction of Dr. Marija Baranac - Stojanović, professor of the Faculty of Chemistry, University of Belgrade
Publications:
- Aleksic, Jovana; Stojanovic, Milovan; Baranac-Stojanovic, Marija, Origin of Fluorine/Sulfur Gauche Effect of β-Fluorinated Thiol, Sulfoxide, Sulfone, and Thionium Ion, Journal of Organic Chemistry (2015), 80(20), 10197-10207.
- Stojanovic, Milovan; Aleksic, Jovana; Baranac-Stojanovic, Marija, The effect of steric repulsion on the torsional potential of n-butane: a theoretical study, Tetrahedron (2015), 71(32), 5119-5123.
- Baranac-Stojanovic, Marija; Aleksic, Jovana; Stojanovic, Milovan, Energy decomposition analysis of gauche preference in 2-haloethanol, 2-haloethylamine (halogen = F, Cl), their protonated forms and anti preference in 1-chloro-2-fluoroethane, RSC Advances (2015), 5 (29), 22980-22995.
- Stojanovic, Milovan; Dzambaski, Zdravko; Bondzic, Bojan; Aleksic, Jovana; Baranac-Stojanovic, Marija, 4-Oxothiazolidines with Exocyclic C=C Double Bond(s): Synthesis, Structure, Reactions and Biological Activity, Current Organic Chemistry (2014), 18(9), 1108-1148. (revijalni rad)
- Khera, Rasheed Ahmad; Ali, Asad; Rafique, Hummera; Hussain, Munawar; Tatar, Jovana; Saeed, Aamer; Villinger, Alexander; Langer, Peter, Suzuki-Miyaura reactions of N-protected tribromopyrazoles. Efficient and site-selective synthesis of 3,4,5-triaryl-pyrazoles, 3,5-diaryl-4-bromopyrazoles and 5-aryl-3,4-dibromopyrazoles, Tetrahedron (2011), 67(29), 5244-5253.
- Baranac-Stojanovic, Marija; Tatar, Jovana; Stojanovic, Milovan; Markovic, Rade, Transformations of 2-alkylidene-4-oxothiazolidine vinyl bromides initiated by bromophilic attack of neutral and anionic nucleophiles, Tetrahedron (2010), 66(34), 6873-6884.
- Tatar, Jovana; Marković, Rade; Stojanović, Milovan; Baranac-Stojanović, Marija, Bromophilic substitution/carbophilic substitution cascade reactions of α,α-dibromo-2-methoxyacetophenone with C-, N- and O-nucleophiles, Tetrahedron Letters (2010), 51(37), 4851-4855.
- Khera, Rasheed Ahmad; Ali, Asad; Hussain, Munawar; Tatar, Jovana; Villinger, Alexander; Langer, Peter, Synthesis of arylated pyrazoles by site-selective Suzuki-Miyaura reactions of tribromopyrazoles, Synlett (2010), (13), 1923-1926.
- Tatar, Jovana; Baranac-Stojanović, Marija; Stojanović, Milovan; Marković, Rade, Reactions of ortho-substituted a,a-dibromoacetophenones with nucleophiles: first examples for combined carbophilic and bromophilic attack on C–Br bond, Tetrahedron Letters (2009), 50, 700-703.
- Baranac-Stojanović, Marija; Tatar, Jovana; Kleinpeter, Erich; Marković, Rade, High-yield synthesis of substituted and unsubstituted pyridinium salts containing a 4-oxothiazolidine moiety, Synthesis (2008), 2117-2121.