Milovan Stojanović

508 total citations
41 papers, 406 citations indexed

About

Milovan Stojanović is a scholar working on Organic Chemistry, Physical and Theoretical Chemistry and Spectroscopy. According to data from OpenAlex, Milovan Stojanović has authored 41 papers receiving a total of 406 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Organic Chemistry, 7 papers in Physical and Theoretical Chemistry and 6 papers in Spectroscopy. Recurrent topics in Milovan Stojanović's work include Synthesis of heterocyclic compounds (15 papers), Synthesis and Properties of Aromatic Compounds (12 papers) and Synthesis and Reactivity of Sulfur-Containing Compounds (11 papers). Milovan Stojanović is often cited by papers focused on Synthesis of heterocyclic compounds (15 papers), Synthesis and Properties of Aromatic Compounds (12 papers) and Synthesis and Reactivity of Sulfur-Containing Compounds (11 papers). Milovan Stojanović collaborates with scholars based in Serbia, New Zealand and Germany. Milovan Stojanović's co-authors include Marija Baranac‐Stojanović, Rade Marković, Peter J. Steel, Erich Kleinpeter, Bojan P. Bondžić, Dragomir Stanisavljev, Dušanka Milojković‐Opsenica, Dragica M. Minić, Dragana Dabić Zagorac and Maja Natić and has published in prestigious journals such as Physical Chemistry Chemical Physics, The Journal of Organic Chemistry and Chemistry - A European Journal.

In The Last Decade

Milovan Stojanović

39 papers receiving 401 citations

Peers

Milovan Stojanović
G. Gayatri India
Bhawani Shankar India
Konstantin Troshin Germany
Alexander Pashenko Ukraine
Phyllis A. Leber United States
Justin R. Griffiths United States
Валентина А. Карноухова Russia
Youssef Arfaoui Tunisia
Julio M. Hernández‐Pérez Mexico
Avene C. Colgan United Kingdom
G. Gayatri India
Milovan Stojanović
Citations per year, relative to Milovan Stojanović Milovan Stojanović (= 1×) peers G. Gayatri

Countries citing papers authored by Milovan Stojanović

Since Specialization
Citations

This map shows the geographic impact of Milovan Stojanović's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Milovan Stojanović with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Milovan Stojanović more than expected).

Fields of papers citing papers by Milovan Stojanović

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Milovan Stojanović. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Milovan Stojanović. The network helps show where Milovan Stojanović may publish in the future.

Co-authorship network of co-authors of Milovan Stojanović

This figure shows the co-authorship network connecting the top 25 collaborators of Milovan Stojanović. A scholar is included among the top collaborators of Milovan Stojanović based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Milovan Stojanović. Milovan Stojanović is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Stojanović, Milovan, et al.. (2024). Solid-state synthesis of polyfunctionalized 2-pyridones and conjugated dienes. Organic & Biomolecular Chemistry. 22(35). 7218–7230.
2.
Baranac‐Stojanović, Marija, et al.. (2024). A theoretical study on application of BN/CC isosterism to modify topology of coronene aromaticity and HOMO–LUMO energy gaps. New Journal of Chemistry. 48(32). 14277–14291. 3 indexed citations
3.
Stojanović, Milovan, et al.. (2021). Singlet/Triplet State Anti/Aromaticity of CyclopentadienylCation: Sensitivity to Substituent Effect. Chemistry. 3(3). 765–782. 9 indexed citations
4.
Baranac‐Stojanović, Marija, et al.. (2021). Revival of Hückel Aromatic (Poly)benzenoid Subunits in Triplet State Polycyclic Aromatic Hydrocarbons by Silicon Substitution. Chemistry - An Asian Journal. 17(4). e202101261–e202101261. 2 indexed citations
5.
Stojanović, Milovan & Marija Baranac‐Stojanović. (2018). Mono BN-substituted analogues of naphthalene: a theoretical analysis of the effect of BN position on stability, aromaticity and frontier orbital energies. New Journal of Chemistry. 42(15). 12968–12976. 21 indexed citations
6.
Stojanović, Milovan, et al.. (2015). Origin of Fluorine/Sulfur Gauche Effect of β-Fluorinated Thiol, Sulfoxide, Sulfone, and Thionium Ion. The Journal of Organic Chemistry. 80(20). 10197–10207. 20 indexed citations
7.
8.
Stojanović, Milovan, et al.. (2015). The effect of steric repulsion on the torsional potential of n-butane: a theoretical study. Tetrahedron. 71(32). 5119–5123. 9 indexed citations
9.
Baranac‐Stojanović, Marija & Milovan Stojanović. (2013). Substituent effects on cyclic electron delocalization in symmetric B- and N-trisubstituted borazine derivatives. RSC Advances. 3(46). 24108–24108. 12 indexed citations
10.
Baranac‐Stojanović, Marija & Milovan Stojanović. (2013). Magnetic Anisotropy of the CC Single Bond. Chemistry - A European Journal. 19(13). 4249–4254. 10 indexed citations
11.
Stojanović, Milovan, Rade Marković, Erich Kleinpeter, & Marija Baranac‐Stojanović. (2011). Synthesis of thiazolidine-fused heterocycles via exo-mode cyclizations of vinylogous N-acyliminium ions. Organic & Biomolecular Chemistry. 10(3). 575–589. 11 indexed citations
12.
Stojanović, Milovan, Rade Marković, Erich Kleinpeter, & Marija Baranac‐Stojanović. (2011). endo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidines. Tetrahedron. 67(49). 9541–9554. 13 indexed citations
13.
Stojanović, Milovan, et al.. (2011). Thermal solid-state Z/E isomerization of 2-alkylidene-4-oxothiazolidines: Effects of non-covalent interactions. Journal of the Serbian Chemical Society. 76(3). 317–328. 5 indexed citations
14.
Baranac‐Stojanović, Marija, et al.. (2010). Transformations of 2-alkylidene-4-oxothiazolidine vinyl bromides initiated by bromophilic attack of neutral and anionic nucleophiles. Tetrahedron. 66(34). 6873–6884. 10 indexed citations
15.
16.
Marković, Rade, Marija Baranac‐Stojanović, Peter J. Steel, Erich Kleinpeter, & Milovan Stojanović. (2006). Stereocontrolled Synthesis of New Tetrahydrofuro[2,3‐d]thiazole Derivatives via Activated Vinylogous Iminium Ions.. ChemInform. 37(13). 1 indexed citations
17.
Marković, Rade, Marija Baranac‐Stojanović, Peter J. Steel, Erich Kleinpeter, & Milovan Stojanović. (2005). Stereocontrolled Synthesis of New Tetrahydrofuro[2,3-d]thiazole Derivatives via Activated Vinylogous Iminium Ions. Heterocycles. 65(11). 2635–2635. 24 indexed citations
18.
Marković, Rade, et al.. (2004). Thionation of N-methyl- and N-unsubstituted thiazolidine enaminones. Journal of the Serbian Chemical Society. 69(11). 909–918. 8 indexed citations
19.
Marković, Rade, et al.. (2003). Regiospecificty in the heterocyclization of β-oxonitriles to 5-substituted 4-oxothiazolidine derivatives. Journal of the Serbian Chemical Society. 68(4-5). 383–390. 1 indexed citations
20.
Marković, Rade, et al.. (2003). High regioselectivity in the heterocyclization of β-oxonitriles to 4-oxothiazolidines: X-ray structure proof. Tetrahedron. 59(39). 7803–7810. 31 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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