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Scientific Publications

International research results and scientific papers

2026
Rávai B., Ujj D.V., Orosz M.J., Revenco E., Béni Sz., Tajti Á., Bálint E.
Pilot-Scale Continuous Flow Synthesis of Capsaicinoids and Their Formulation with Cyclodextrins
ACS Omega, 11(3), 4570–4580
DOI: 10.1021/acsomega.5c10910 →
Samra A., Radoua A., Sila Tanaydin E., Alrustom B., Bordessoules M., Fischer T., Callot M., Georgsson S., Rávai B., Mátravölgyi B. et al.
Quantifying loss of cell viability or adhesion using methylene blue
Methods in Cell Biology, 206, 125–143
DOI: 10.1016/bs.mcb.2026.02.015 →
Gerő V., Steinsits D., Tamás Szabó P., Bálint E.
Flow Chemistry Meets Green Solvents: Telescoped Synthesis of Triazolyl Phosphoramidates and Phosphinamides in γ-Valerolactone
ChemSusChem, 19(9), e70680
DOI: 10.1002/cssc.70680 →
Ujj D.V., Kasal P., Fejős I., Béni Sz., Kardos J., Benkovics G., Bálint E., Mátravölgyi B.
Complexation of Citalopram with β-Cyclodextrin, Mono-Subetadex and Subetadex
ACS Omega, 11(16), 24323–24333
DOI: 10.1021/acsomega.5c13544 →
Gyöngyössy Á., Orosz J.M., Pusztai É., Pomberger A., Wigh D., Bálint E.
Flow synthesis of heterocyclic capsaicinoid analogues supported by complementary DoE and Bayesian optimization
Chemical Engineering Science (2026)
DOI: 10.26434/chemrxiv.15001104/v1 →
2025
Mika L.T., Árvai Cs., Bálint E., Rávai B.
Evaluating Greenness of Solvents
Encyclopedia of Green Chemistry, Vol. 3, pp. 1–16, Elsevier
DOI: 10.1016/B978-0-443-15742-4.00051-X →
Rávai B., Németh Á.S., Kelemen Zs., Bálint E.
Microwave-Assisted Multicomponent Synthesis of Spirooxindole Dihydropyridine Bisphosphonates
European Journal of Organic Chemistry, 28(6), e202400873
DOI: 10.1002/ejoc.202400873 →
Rávai B., Kese I., Szakály P.S., Herr D., Iványi R., Bálint E., Szőcs L.
Mono-(6-sulfinic acid)-Sugammadex: A newly identified cyclodextrin-based oxidative impurity in industrial production
Carbohydrate Polymers, 362, 123659
DOI: 10.1016/j.carbpol.2025.123659 →
Steinsits D., Rávai B., Kelemen Zs., Hackler L., Vernyik V., Puskás L.G., Bálint E.
3,3-Bis(hydroxyaryl)oxindoles and Spirooxindoles Bearing a Xanthene Moiety
Journal of Organic Chemistry, 90(19), 6454–6467
DOI: 10.1021/acs.joc.5c00270 →
Nguyen H.H.T., Bálint E., Mátravölgyi B.
Time-Dependent Resolution of an Atropisomeric 1-Arylpyrrole by a Novel 1-Arylethylamine Saltforming Agent
Chirality, 37(10), e70054
DOI: 10.1002/chir.70054 →
2024
Rávai B., Popovics-Tóth N., Komka K., Csontos I., Szokol B., Őrfi Z., Őrfi L., Bálint E.
Phosphoryl- or phosphinoyl-functionalized benzo[de]isoquinolinones
Reaction Chemistry & Engineering, 9(3), 583–593
DOI: 10.1039/D3RE00489A →
Rávai B., Orosz M.J., Péterfi O., Galata D.L., Bálint E.
Flow chemical laboratory practice for undergraduate students: synthesis of paracetamol
Journal of Flow Chemistry, 14(2), 409–415
DOI: 10.1007/s41981-023-00303-y →
Orosz M.J., Rávai B., Mátravölgyi B., Bálint E.
Flow Synthesis of Capsaicin and Capsaicinoid Analogues
ACS Sustainable Chemistry & Engineering, 12(20), 7913–7923
DOI: 10.1021/acssuschemeng.4c01839 →
Szabó K., Kelemen Zs., Szabó P.T., Bálint E.
Synthetic and mechanistic studies of the multicomponent reaction
Reaction Chemistry & Engineering, 9(12), 3222–3230
DOI: 10.1039/D4RE00387J →
2023
Popovics-Tóth N., Bao T.D.T., Tajti Á., Mátravölgyi B., Kelemen Zs., Perdih F., Hackler L., Puskás L.G., Bálint E.
Three-Component Reaction of 3-Formyl-6-Methylchromone, Primary Amines, and Secondary Phosphine Oxides
ACS Omega, 8(2), 2698–2711
DOI: 10.1021/acsomega.2c07333 →
Orosz J.M., Ujj D., Kasal P., Benkovics G., Bálint E.
Continuous flow synthesis of 6-monoamino-6-monodeoxy-β-cyclodextrin
Beilstein Journal of Organic Chemistry, 19, 294–302
DOI: 10.3762/bjoc.19.25 →
2022
Popovics-Tóth N., Turpanova M., Németh K., Hackler Jr. L., Puskás L.G., Bálint E.
Synthesis of arylphosphinoyl-functionalized dihydroisoquinolines by Reissert-type reaction
Tetrahedron, 111, 132720
DOI: 10.1016/j.tet.2022.132720 →
Popovics-Tóth N., Bálint E.
Multicomponent Synthesis of Potentially Biologically Active Heterocycles Containing a Phosphonate or a Phosphine Oxide Moiety
Acta Chimica Slovenica, 69, 735–755
DOI: 10.17344/acsi.2022.7648 →
Szabó K.E., Akali R., Tajti Á., Popovics-Tóth N., Bálint E.
Microwave-assisted synthesis of α-aminophosphonate-chromone hybrids using Kabachnik-Fields Reaction
Arkivoc, 3, 256–271
DOI: 10.24820/ark.5550190.p011.887 →
Popovics-Tóth N., Tajti Á., Hümpfner E., Bálint E.
Synthesis of 3,4-Dihydropyrimidin-2(1H)-one-phosphonates by the Microwave-Assisted Biginelli Reaction
Catalysts, 11(1), 45
DOI: 10.3390/catal11010045 →
2021
Tajti Á., Szabó K.E., Popovics-Tóth N., Iskanderov J., Perdih F., Hackler L., Kari B., Puskás L.G., Bálint E.
PMDTA-catalyzed multicomponent synthesis and biological activity of 2-amino-4H-chromenes containing a phosphonate or phosphine oxide moiety
Organic & Biomolecular Chemistry, 19, 6883–6891
DOI: 10.1039/D1OB01204E →
Popovics-Tóth N., Rávai B., Tajti Á., Varga B., Bagi P., Perdih F., Szabó P.T., Hackler L., Puskás L.G., Bálint E.
Three-component synthesis, utilization and biological activity of phosphinoyl-functionalized isoindolinones
Organic & Biomolecular Chemistry, 19(40), 8754–8760
DOI: 10.1039/d1ob01610e →
Tripolszky A., Tóth E., Szabó P.T., Hackler L., Kari B., Puskás L.G., Bálint E.
Synthesis and In Vitro Cytotoxicity and Antibacterial Activity of Novel 1,2,3-Triazol-5-yl-Phosphonates
Molecules, 25(11), 2643
DOI: 10.3390/molecules25112643 →
Tajti Á., Tóth N., Rávai B., Csontos I., Szabó P.T., Bálint E.
Study on the Microwave-Assisted Batch and Continuous Flow Synthesis of N-Alkyl-Isoindolin-1-One-3-Phosphonates
Molecules, 25(14), 3307
DOI: 10.3390/molecules25143307 →
2018
Mátravölgyi B., Hergert T., Bálint E., Bagi P., Faigl F.
Access to Fluorazones by Intramolecular Dehydrative Cyclization of Aromatic Tertiary Amides
Journal of Organic Chemistry, 83(4), 2282–2292
DOI: 10.1021/acs.joc.7b03176 →
Bálint E., Tajti Á., Tripolszky A.
Synthesis of α-aminophosphonates by the Kabachnik–Fields reaction and by the Pudovik reaction
Organophosphorus Chemistry: Novel Developments, pp. 108–147, De Gruyter
DOI: 10.1515/9783110535839-006 →

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