Publications

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Journal Article
S. B. Ötvös, Szloszár, A., Mándity, I. M., and Fülöp, F., Heterogeneous Dipeptide-Catalyzed a-Amination of Aldehydes in a Continuous-Flow Reactor: Effect of Residence Time on Enantioselectivity, Advanced Synthesis & Catalysis, vol. 357, pp. 3671–3680, 2015.
S. B. Otvos, Mándity, I. M., and Fülöp, F., Highly Efficient 1,4-Addition of Aldehydes to Nitroolefins: Organocatalysis in Continuous Flow by Solid-Supported Peptidic Catalysts, ChemSusChem, vol. 5, pp. 266–269, 2012.
L. Kiss, Mándity, I. M., and Fülöp, F., Highly functionalized cyclic beta-amino acid moieties as promising scaffolds in peptide research and drug design., Amino Acids, vol. 49, p. 1441, 2017.
C. - T. Hsieh, Ötvös, S. B., Wu, Y. - C., Mándity, I. M., Chang, F. - R., and Fülöp, F., Highly Selective Continuous-Flow Synthesis of Potentially Bioactive Deuterated Chalcone Derivatives, ChemPlusChem, vol. 80, pp. 859–864, 2015.
S. B. Otvos, Mándity, I. M., and Fülöp, F., Highly selective deuteration of pharmaceutically relevant nitrogen-containing heterocycles: a flow chemistry approach, Molecular Diversity, vol. 15, pp. 605–611, 2011.
R. Samavati, Zador, F., Szucs, E., Tuka, B., Martos, D., Veres, G., Gaspar, R., Mándity, I. M., Fülöp, F., Vécsei, L., Benyhe, S., and Borsodi, A., Kynurenic acid and its analogue can alter the opioid receptor G-protein signaling after acute treatment via NMDA receptor in rat cortex and striatum, Journal of the Neurological Sciences, vol. 376, pp. 63–70, 2017.
I. Cs. Szigyártó, Mihály, J., Wacha, A., Bogdán, D., Juhász, T., Kohut, G., Schlosser, G., Zsila, F., Urlacher, V., Varga, Z., Fülöp, F., Bóta, A., Mándity, I., and Beke-Somfai, T., Membrane active Janus-oligomers of β $^\textrm3$ -peptides, Chemical Science, vol. 11, pp. 6868–6881, 2020.
I. M. Mándity, Nagy hatékonyságú kémiai átalakítások folyamatos áramban : védőcsoport-eltávolítás, deuterálás és organokatalízis, Magyar Kémikusok Lapja, vol. 67, pp. 336–337, 2012.
S. Ötvös, Mándity, I. M., and Fülöp, F., Organokatalízis folyamatos áramú reaktorban, Magyar Kémikusok Lapja, vol. 67, pp. 143–146, 2012.
I. M. Mándity and Fülöp, F., An overview of peptide and peptoid foldamers in medicinal chemistry, Expert Opinion on Drug Discovery, vol. 10, pp. 1163–1177, 2015.
A. Szabados-Nacsa, Sipos, P., Martinek, T., Mándity, I. M., Blazso, G., Balogh, A., Szabo-Revesz, P., and Aigner, Z., Physico-chemical characterization and in vitro/in vivo evaluation of loratadine: dimethyl-β-cyclodextrin inclusion complexes, Journal of Pharmaceutical and Biomedical Analysis, vol. 55, pp. 294–300, 2011.
F. S. Ekholm, Mándity, I. M., Fülöp, F., and Leino, R., Rapid, simple, and efficient deprotection of benzyl/benzylidene protected carbohydrates by utilization of flow chemistry, Tetrahedron Letters, vol. 52, pp. 1839–1841, 2011.
A. Hetenyi, Szakonyi, Z., Mándity, I. M., Szolnoki, E., Toth, G. K., Martinek, T. A., and Fülöp, F., Sculpting the beta-peptide foldamer H12 helix via a designed side-chain shape, Chemical Communications, pp. 177–179, 2009.
M. A. T, Hetenyi, A., Fulop, L., Mándity, I. M., K. G, T., Dékány, I., and Fülöp, F., Secondary structure dependent self-assembly of beta-peptides into nanosized fibrils and membranes, Angewandte Chemie - International Edition, vol. 45, pp. 2396–2400, 2006.
I. M. Mándity, Martinek, T. A., Darvas, F., and Fülöp, F., A simple, efficient, and selective deuteration via a flow chemistry approach, Tetrahedron Letters, vol. 50, pp. 4372–4374, 2009.
M. F., Mándity, I. M., R., S., and F., F., Stereocontrolled synthesis of five diastereomers of trimethyl 3-aminocyclopentane-1,2,4-tricarboxylates, Tetrahedron Letters, vol. 54, pp. 3769–3772, 2013.
I. M. Mándity, Ötvös, S. B., and Fülöp, F., Strategic application of residence time control in continuous flow reactors, Chemistry Open, vol. 4, pp. 212–223, 2015.
A. Szloszár, Mándity, I. M., and Fülöp, F., Sustainable synthesis of N-methylated peptides in a continuous-flow fixed bed reactor, Journal of Flow Chemistry, pp. 1–7, 2018.
B. Kazi, Kiss, L., Forro, E., Mándity, I. M., and Fülöp, F., Synthesis of conformationally constrained, orthogonally protected 3-azabicyclo[3.2.1]octane beta-amino esters, ARKIVOC, vol. 2010, pp. 31–39.
A. Hetenyi, Mándity, I. M., Martinek, T., Toth, G. K., and Fülöp, F., TRUE FOLDING OF CONFORMATIONALLY CONSTRAINED beta-PEPTIDES: CHAIN LENGTH-DEPENDENT SECONDARY STRUCTURE, Journal of Peptide Science, vol. 10, p. 273, 2004.
Ł. Berlicki, Pilsl, L., Weber, E., Mándity, I. M., Cabrele, C., A. T, M., Fülöp, F., and Reiser, O., Unique α,β- and α,α,β,β-peptide foldamers based on cis-β-aminocyclopentanecarboxylic acid, Angewandte Chemie - International Edition, vol. 51, pp. 2208–2212, 2012.
E. Vass, Strijowski, U., Wollschlager, K., Mándity, I. M., Szilvagyi, G., Jewginski, M., Gaus, K., Royo, S., Majer, Z., Sewald, N., and Hollósi, M., VCD studies on cyclic peptides assembled from L-alpha-amino acids and a trans-2-aminocyclopentane- or trans-2-aminocyclohexane carboxylic acid, Journal of Peptide Science, vol. 16, pp. 613–620, 2010.

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