Zobrazeno 1 - 10
of 378
pro vyhledávání: '"Csaba Szántay"'
Publikováno v:
Arkivoc. 2022:240-255
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b597d59b8bfaebd2b1cb916aed1a107
https://doi.org/10.24820/ark.5550190.p011.884
https://doi.org/10.24820/ark.5550190.p011.884
Autor:
Viktor Ilkei, András Spaits, Anita Prechl, Áron Szigetvári, Zoltán Béni, Miklós Dékány, Csaba Szántay Jr, Judit Müller, Árpád Könczöl, Ádám Szappanos, Attila Mándi, Sándor Antus, Ana Martins, Attila Hunyadi, György Tibor Balogh, György Kalaus (†), Hedvig Bölcskei, László Hazai, Tibor Kurtán
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2523-2534 (2016)
Starting from racemic naringenin ((±)-1), a mixture of dracocephin A stereoisomers 6-(2”-pyrrolidinone-5”-yl)naringenin (±)-2a–d and its regioisomer, dracocephin B 8-(2”-pyrrolidinone-5”-yl)naringenin (±)-3a–d originally isolated from
Externí odkaz:
https://doaj.org/article/823146f9413e436d88e1a1a187962d5a
Autor:
András Keglevich, Leonetta Dányi, Alexandra Rieder, Dorottya Horváth, Áron Szigetvári, Miklós Dékány, Csaba Szántay, Ahmed Dhahir Latif, Attila Hunyadi, István Zupkó, Péter Keglevich, László Hazai
Publikováno v:
Molecules, Vol 25, Iss 4, p 1010 (2020)
New Vinca alkaloid derivatives were synthesized to improve the biological activity of the natural alkaloid vindoline. To this end, experiments were performed to link vindoline with various structural units, such as amino acids, a 1,2,3-triazole deriv
Externí odkaz:
https://doaj.org/article/8205cc99dfa644c4aaafdb1e0368d56d
Autor:
Szabolcs Mayer, Péter Keglevich, Péter Ábrányi-Balogh, Áron Szigetvári, Miklós Dékány, Csaba Szántay, László Hazai
Publikováno v:
Molecules, Vol 25, Iss 4, p 888 (2020)
Chrysin is a naturally occurring flavonoid with mild anticancer activity. In this paper we report the synthesis of new chrysin derivatives alkylated with N-phenylchloroacetamides in position 7. A novel method was developed for the preparation of 7-am
Externí odkaz:
https://doaj.org/article/9545a6a8a59343779b95ac4d3b037628
Autor:
Ewald Moser, Csaba Szántay Jr.
Publikováno v:
Frontiers in Physics, Vol 6 (2018)
Externí odkaz:
https://doaj.org/article/0b55c399c4684839aedb5652e92c5475
Autor:
Csaba Szántay Jr., Ewald Moser
Publikováno v:
Frontiers in Physics, Vol 6 (2018)
Externí odkaz:
https://doaj.org/article/d3436f64d1df4f45a34d3ad2a393fd6e
Autor:
Balázs Krámos, Zoltán Szakács, Imre Bata, Ferenc Baska, Csaba Szántay, Krisztina Temesvári, Krisztina Vukics, Éva Bozó, Zoltán Béni, Sándor Lévai, Katalin Domány-Kovács, Ildikó Magdó, Elemér Vass, Zsolt Szeleczky, István Greiner, János Kóti
Publikováno v:
Journal of Medicinal Chemistry. 64:10445-10468
A new class of selective vasopressin receptor 1A (V1A) antagonists was identified, where "methyl-scan" was performed around the benzene ring of the 5-hydroxy-triazolobenzazepine core. This led to the synthesis of two 10-methyl derivatives, each posse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1131c30041ae03eeaa3142e7f9dce5a
https://doi.org/10.1021/acs.jmedchem.1c00863
https://doi.org/10.1021/acs.jmedchem.1c00863
Autor:
Áron Szigetvári, Csaba Szántay
Publikováno v:
Magyar Kémiai Folyóirat. 126:135-146
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dde452a210f3f49718fa15c9daa5f149
https://doi.org/10.24100/mkf.2020.04.134
https://doi.org/10.24100/mkf.2020.04.134
Publikováno v:
Molecules, Vol 17, Iss 5, Pp 5893-5914 (2012)
The synthetic investigation of biologically active natural compounds serves two main purposes: (i) the total synthesis of alkaloids and their analogues; (ii) modification of the structures for producing more selective, more effective, or less toxic d
Externí odkaz:
https://doaj.org/article/a81c730409fe4158aa3b624c4191cc86
Autor:
András Keglevich, Szabolcs Mayer, Réka Pápai, Áron Szigetvári, Zsuzsanna Sánta, Miklós Dékány, Csaba Szántay, Péter Keglevich, László Hazai
Publikováno v:
Molecules, Vol 23, Iss 10, p 2574 (2018)
Our successful work for the synthesis of cyclopropanated vinblastine and its derivatives by the Simmons–Smith reaction was followed to build up further three-membered rings into the 14,15-position of the vindoline part of the dimer alkaloid. Haloge
Externí odkaz:
https://doaj.org/article/af881658737844deb1c489859450850b