V3 Gašparová R.: Natural compounds with oxepinochromene scaffold. Structure, source, biological activity and synthesis. Chemistry and Biodiversity, 2022, 19, e202200507.

V3 Tokárová Z., Gašparová R., Kabaňová M., Gašparová M., Balogh R.: Hemetsberger–Knittel and Ketcham Synthesis of Heteropentalenes with Two (1:1), Three (1:2)/(2:1) and Four (2:2) Heteroatoms. Reactions 2023, 4, 254-273.

V2 Gašparová R., Villemin D., Bar N.: Microwave activation: solventless catalysed synthesis of cross conjugated dienones of Tropinone. Chemistry Proceedings 2023, 14, 28.

V2 Gašparová R.: In Silico Studies of Khellin and Related Furochromenes by Modified POM Analysis. Chemistry proceedings, 2024, 6, 2.

V2 Gašparová R.: Synthesis of tricyclic 5:5:6 heterocycles with three heteroatoms. In: Applied Natural Sciences 2023 : Book of Abstracts : 1. vyd. - Trnava : Fakulta prírodných vied, 2023. - ISBN 978-80-572-0357-5, s. 13-13.

V2 Gašparová R., Kabaňová N.: In Silico Pharmacological Prediction of Capitavine, Buchenavianine and Related Flavonoid Alkaloids. Chemistry proceedings, 2024, 6, 55.

Heuzé B; Gasparova , R.; Heras M; Masson, S. Tetrahedron Lett., 2000, 41, 7327 -7331.

ohlasy:

• Bingham, N.M.; Abousalman-Rezvani, Z.; Abousalman-Rezvani, Z.; Collins, K.; Roth, P.J.: Thiocarbonyl chemistry in polymer science. POLYMER CHEMISTRY 13, 2022, 2880-2901
• Willcock, H; O'Reilly, RK. End group removal and modification of RAFT polymers. Polymer Chem. 2010,‏ 1, 149-157
• Boyer, C; Stenzel, MH.; Davis, TP. Building Nanostructures Using RAFT Polymerization. J. Popymer Sci. A - Polym. Chem. 2011,‏ 49,‏ 551-595
• Moad, G Rizzardo, E; Thang, SH. End-functional polymers, thiocarbonylthio group removal/transformation and reversible addition-fragmentation-chain transfer (RAFT) polymerization. Polymer Int. 2011,‏ 60,‏ 9-25
• Sinnwell S., Sinatschke C. V., Junkers T., Stenzel M.H., Barner-Kowollik C.: A Study into the Stability of 3,6-Dihydro-2H-thiopyran Rings: Key Linkages in the RAFT Hetero-Diels - Alder Click Concept. Macromolecules 41, 2008, 7904-7912.

Gasparova, R., Lacova, M;. El-Shaaer, H M; Odlerova Z. Synthesis and antimycobacterial activity of some new 3-heterocyclic substituted chromones. Farmaco 1997, 52, 251–253.

ohlasy:

• Ballell, L; Field, RA; Duncan, K; Young, RJ. New small-molecule synthetic antimycobacterials. Antimicrob. Agents Chemtot. 2005, 49, 2153-2163
• Augustynowicz-Kopec E., Zwolska Z., Orzeszko A., Kazimierczuk Z.: Synthesis and Antimycobacterial Activity of Selected Nitrobenzyloxylated Benzotriazoles. Acta Polon. Pharm. 65, 2008, 435-439.    
• Randhavane P.V., Karale B.K.:Synthesis and biological screening of different heterocycles derived from 4-(pyridine-2-yl)benzaldehyde. Heterocycl. Commun. 14, 2008, 433-442.
• El-Sayed A.T., Tes A.: Synthesis and fungicidal activity of some new 4H-Chromen-4-ones containing some 1,3-thiazole, 1,3-thiazine, 1,2,4-triazole and 1,2,4-triazine moieties. Phosphorus, sulfur. 182, 2007, 1717-1726.
• Harizi A, Zantour H.: Synthesis of fostedil (diethyl 4-(2-benzothiazolyl)benzylphosphonate) from N-acylimidates.  Phosphorus, Sulfur.179, 2004, 1883-1891.

Stankovičová H, Gašparová R, Lácová M, Chovancová J. Reaction of 4-Oxochromene-3-carboxaldehydes with Primary Amides and Benzotriazole or 1H-1,2,4-Triazole.Collect. Czech. Chem. Commun. 1997, 62, 781-790.

ohlasy:

• Korzhenko, K.S.; Osipov, D.V.; Osyanin, V.A.; Klimochkin, Y.N.: Divergent Pathways for Reactions of 3-Formylchromone with Cyclic Secondary Amines in Alcoholic Media. SYNOPEN 3, 2019, 164-168
• al-Rashida, M; Ashraf, M;  Hussain, B.; Nagra, S.A.; Abbas, G. : Discovery of new chromone containing sulfonamides as potent inhibitors of bovine cytosolic carbonic anhydrase. BIOORGANIC & MEDICINAL CHEMISTRY 19, 2011, 3367-3371
• Lidstrom, P; Tierney, J; Wathey, B; Westman, J. Microwave assisted organic synthesis - a review. Tetrahedron 2001, 57, 9225-9283.
• Ghosh C.K., Patra A.: Chemistry and Application of 4-Oxo-4H-1-benzopyran-3-carboxaldehyde. J. Heterocycl. Chem. 45, 2008, 1529-1547.

Lácová M., Gašparová R., Koiš P., Boháč A., El-Shaaer H.M.: A Facile Route to Phenyl, Phenylsulfanyl and Phenylselanyl Substituted Pyrano[3,2-c]chromenes. Tetrahedron, 2010, 66, 1410-1419.

ohlasy:

• Chernov, N.M.; Shutov, R.V.;  Sipkina, N.Y. ; Krivchun, M., Yakovlev, I.P.: A Flexible Synthetic Approach to Fluorescent Chromeno[4,3-b]]pyridines and Pyrano[3,2-c]chromenes from Electron-Deficient 3-Vinylchromones. CHEMPLUSCHEM 86 , 2021, 1256-1266
• Dolatkhah, Z; Javanshir, S; Sadr, A.S., Hosseini, J ; Sardari, S.: Synthesis, Molecular Docking, Molecular Dynamics Studies, and Biological Evaluation of 4H-Chromone-1,2,3,4-tetrahydropyrimidine-5-carboxylate Derivatives as Potential Antileukemic Agents. JOURNAL OF CHEMICAL INFORMATION AND MODELING 57 (6) , 2017, 1246-1257
• Parmar, B.D.; Sutariya, T.R.;  Brahmbhatt, GC ; Parmar, NJ ; Kant, R .; Gupta, V.K.: A Base-Catalyzed, Domino Aldol/hetero-Diels-Alder Synthesis of Tricyclic Pyrano[3,4-c]chromenes in Glycerol. JOURNAL OF ORGANIC CHEMISTRY 81, 2016, 4955-4964
• Rajkumar, K.; Hariprasad, K.S.; Sridhar, B.; Raju, B.C.: Convenient synthesis of 4H-chromenyl-tetrahydro-2H-pyrancarboxylates and cleavage of chromone and pyran rings leading to 5-(2-hydroxybenzoyl)-2-(trifluoromethyl)-1,2-dihydropyridine-3-carboxylates. SYNTHETIC COMMUNICATIONS 46, 2016,1963-1971
• Akkurt, M; Horton, P.N.; Mohamed, S.K., Younes, S.H.H.; Albayati, M.R.: Crystal structure of 3-amino-1-(4-chlorophenyl)-1H-benzo[f]chromene-2-carbonitrile. ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONSarrow_ 71, 2015,O481-U311

Gašparová R., Lácová M.: Reactions of 3-Formylchromone with Active Methylene and Methyl Compounds and Some Subsequent Reactions of the Resulting Condensation Products. Molecules 2005,10, 928-951.

ohlasy:

• Alizadeh, A.,   Rostampoor, A.: Convenient Synthesis of Functionalized Tetracyclic Dihydrochromeno[2,3-b ]pyrrolo[3,4-e ]pyridine-triones via Four-Component Reactions. SYNTHESIS-STUTTGART 56, 2024 ,267-274
• Alsehli, M.H.; Seth, D.S.; El-Gaby, M.S.A.; Okasha, R.M.; Hagar, M.; Afifi, T.H.; Naqvi, A.: DFT and In-silico Investigations, along with In-vitro Antitumor and Antimicrobial Assessments of Pharmacological Molecules. CURRENT ORGANIC SYNTHESIS 20 (5) , 2023, 523-545
• Salvador J. A. R., Pinto R. M. A., Silvestre S.M.: Recent Advances of Bismuth(III) Salts in Organic Chemistry: Application to the Synthesis of Heterocycles of Pharmaceutical Interest. Curr. Org. Synth. 6, 2009,  426-470.
• Jabeen S., Palmer R.A., Potter B.S., Helliwell M., Dines T.J., Chowdhry B.Z.: Low Temperature Crystal Structures of Two Rhodanine Derivatives, 3-Amino Rhodanine and 3-Methyl Rhodanine: Geometry of the Rhodanine Ring. J. Chem. Crystallogr. 39, 2009, 151-156.
• Sosnovskikh V.Y., Moshkin V.S., Kodess M.I.: A reinvestigation of the reactions of 3-substituted chromones with hydroxylamine. Unexpected synthesis of 3-amino-4H-chromeno[3,4-d]-isoxazol-4-one and 3-(diaminomethylene)chroman-2,4-dione. Tetrahedron Lett. 49, 2008, 6856-6859.
• Sosnovskikh V.Y., Moshkin V.S., Kodess M.I.: Reactions of 3-(polyfluoroacyl)chromones with hydroxylamine: synthesis of novel R-F-containing isoxazole and chromone derivatives. Tetrahedron 64, 2008, 7877-7889.

APVV-16-0173 Terapeutické alternatívy k liečbe rezistentných bakteriálnych infekcií. –2017-2020

APVV-18-0016 Molekulové nanomagnety zložené z komplexov prechodných kovov – 2019-2023

VEGA 1/0534/16 Nové zlúčeniny s aplikačným potenciálom –2016-2019

Operational Programme Integrated Infrastructure for the project: Long-term strategic research of prevention, intervention and mechanisms of obesity and its comorbidities, IMTS: 313011V344 (2019-2023).