Tudóstér: Juhászné Tóth Éva publikációi

Juhász-Tóth, É., Malecz, Á., Tóth, M., Homolya, Á., Kaszás, T., Somsák, L., Juhász, L.: 2-Iodo-1-C-acceptor-substituted glycals: synthesis and transformation into 1,2-C,Cdisubstituted glycals via Suzuki-Miyaura coupling reaction.
New Journal of Chemistry 47 (42), 19376-19388, 2023.

Kaszás, T., Szakács, B., Juhász-Tóth, É., Cservenyák, I., Kovács, T., Juhász, L., Somsák, L., Tóth, M.: Coupling of N-Tosylhydrazones with Tetrazoles: A Regioselective Synthesis of 2,5-Disubstituted-2H- Tetrazoles.
European Journal of Organic Chemistry 2022 (42), e202201103, 2022.

Bokor, É., Ferenczi, A., Hashimov, M., Juhász-Tóth, É., Götz, Z., Zaki, A., Somsák, L.: First Synthesis of 3-Glycopyranosyl-1,2,4-Triazines and Some Cycloadditions There of.
Molecules. 27 (22), 1-16, 2022.

Homolya, L., Antal, D., Nagy, M., Juhász-Tóth, É., Tóth, M., Bényei, A., Somsák, L., Juhász, L.: Reactions of 1-C-acceptor-substituted glycals with nucleophiles under acid promoted (Ferrier-rearrangement) conditions.
Carbohydr. Res. 519 1-10, 2022.

Kaszás, T., Cservenyák, I., Juhász-Tóth, É., Kulcsár, A., Granatino, P., Nilsson, U., Somsák, L., Tóth, M.: Coupling of N-tosylhydrazones with tetrazoles: synthesis of 2-beta-d-glycopyranosylmethyl-5-substituted-2H-tetrazole type glycomimetics.
Org. Biomol. Chem. 19 (3), 605-618, 2021.

Nagy, L., Béke, F., Juhász, L., Kovács, T., Juhász-Tóth, É., Docsa, T., Tóth, A., Gergely, P., Somsák, L., Bai, P.: Glycogen phosphorylase inhibitor, 2,3-bis[(2E)-3-(4-hydroxyphenyl)prop-2-enamido] butanedioic acid (BF142), improves baseline insulin secretion of MIN6 insulinoma cells.
PLoS One. 15 (9), 1-15, 2020.

Somsák, L., Bokor, É., Juhász, L., Kun, S., Lázár, L., Juhász-Tóth, É., Tóth, M.: New syntheses towards C-glycosyl type glycomimetics.
Pure Appl. Chem. 91 (7), 1159-1175, 2019.

Kantsadi, A., Bokor, É., Kun, S., Stravodimos, G., Chatzileontiadou, D., Leonidas, D., Juhász-Tóth, É., Szakács, A., Batta, G., Docsa, T., Gergely, P., Somsák, L.: Synthetic, enzyme kinetic, and protein crystallographic studies of C-[béta]-D-glucopyranosyl pyrroles and imidazoles reveal and explain low nanomolar inhibition of human liver glycogen phosphorylase.
Eur. J. Med. Chem. 123 737-745, 2016.

Juhász-Tóth, É., Favi, G., Attanasi, O., Bényei, A., Patonay, T.: Alpha-Azido Ketones, Part 8: Base-Induced Coupling of Alpha-Azido Ketones with a 1,2-Diaza-1,3-diene as a Michael Acceptor.
Synlett. 25 (14), 2001-2004, 2014.

Patonay, T., Kónya, K., Juhász-Tóth, É.: Syntheses and transformations of alpha-azido ketones and related derivatives.
Chem. Soc. rev. 40 (5), 2797-2847, 2011.

Patonay, T., Micskei, K., Juhász-Tóth, É., Fekete, S., Pardi-Tóth, V.: Alpha-Azido ketones, Part 6.: Reduction of acyclic and cyclic alpha-azido ketones into alpha-amino ketones : old problems and new solutions.
Arkivoc. 270-290, 2009.

Patonay, T., Jekő, J., Juhász-Tóth, É.: Alpha-Azido Ketones, 5.: Synthesis of highly substituted 2H-Azirine-2-carboxylates via 3-Azido-4-oxobut-2-enoates.
Eur. J. Org. Chem. 2008 (8), 1441-1448, 2008.

Gulácsi, K., Juhász-Tóth, É., Juhász, L., Somsák, L., Tóth, M.: Szerves kémiai praktikum III..
Debreceni Egyetem Kossuth Egyetemi Kiadó, Debrecen, 331 p., 2006. ISBN: 9789634732464

Patonay, T., Juhász-Tóth, É., Bényei, A.: Base-induced coupling of alpha-azido ketones with aldehydes: an easy and efficient route to trifunctionalized synthons 2-azido-3-hydroxy ketones, 2-acylaziridines, and 2-acylspiroaziridines.
Eur. J. Org. Chem. 2002 (2), 285-295, 2002.

Juhász-Tóth, É., Patonay, T.: Synthesis of tetrafunctionalized 2-azido-3-hydroxy-1,4-diones and their transformation into 5-substituted 3-acylisoxazoles.
Eur. J. Org. Chem. 2002 (17), 3055-3064, 2002.