Zobrazeno 1 - 10
of 87
pro vyhledávání: '"Tamás Holczbauer"'
Publikováno v:
Symmetry, Vol 15, Iss 9, p 1714 (2023)
Carbohydrate-based macrocycles can be enantioselective catalysts in certain reactions. Previously, it was proven that the carbohydrate moiety could affect the catalytic activity of the monoaza-15-crown-5 type macrocycles derived from sugars. Accordin
Externí odkaz:
https://doaj.org/article/aba0addec3aa48e78f218782441ae77d
Unsymmetrical Thienopentalenes: Synthesis, Optoelectronic Properties, and (Anti)aromaticity Analysis
Autor:
Tamás Gazdag, Péter J. Mayer, Péter Pál Kalapos, Tamás Holczbauer, Ouissam El Bakouri, Gábor London
Publikováno v:
ACS Omega, Vol 7, Iss 10, Pp 8336-8349 (2022)
Externí odkaz:
https://doaj.org/article/8d0ff14d91914c1bbf25d4fb49100a6e
Autor:
Bence Varga, Levente Buna, Daniella Vincze, Tamás Holczbauer, Béla Mátravölgyi, Elemér Fogassy, György Keglevich, Péter Bagi
Publikováno v:
Molecules, Vol 28, Iss 4, p 1584 (2023)
A focused library of 1-adamantyl arylthiophosphonates was prepared in racemic form. An enantioseparation method was developed for P-stereogenic thiophosphonates using (S)-1-phenylethylamine as the resolving agent. Under optimized conditions, three ou
Externí odkaz:
https://doaj.org/article/0d73e80b7d014f33bdbd5bff4daf3d1c
Publikováno v:
ARKIVOC, Vol 2016, Iss 3, Pp 242-261 (2016)
Externí odkaz:
https://doaj.org/article/186ea92ceff649e2ac95ed75ac9bbe9b
Autor:
Angelika Thurner, Bernadett Vas-Feldhoffer, Éva Bottka, Tamás Holczbauer, Miklós Nyerges, Ferenc Faigl
Publikováno v:
ARKIVOC, Vol 2015, Iss 4, Pp 80-96 (2015)
Externí odkaz:
https://doaj.org/article/2ad5d6296d28491893d482a422c8109b
Publikováno v:
The Journal of Organic Chemistry. 88:6182-6191
Publikováno v:
Synthetic Communications. 52:1956-1966
Autor:
Bence Varga, Daniella Vincze, Hajnalka Pető, Levente Buna, János Pauló, Tamás Holczbauer, Béla Mátravölgyi, László Hegedűs, Elemér Fogassy, György Keglevich, Péter Bagi
Publikováno v:
Organic Chemistry Frontiers. 9:2797-2807
An enantioseparation method for the preparation of P-stereogenic H-phosphinates was elaborated. In stereoselective reactions, various chiral P-stereogenic compounds were prepared and their applications as chiral NMR solvating agents were assessed.
Autor:
Péter J. Mayer, Bence B. Botlik, Enikő Meiszter, Krisztina Németh, Christian J. Schürmann, Tamás Holczbauer, Gábor London
Publikováno v:
Computational and Theoretical Chemistry. 1224:114113
Autor:
Tamás Holczbauer, Bence Varga, Réka Herbay, Elemér Fogassy, György Keglevich, Péter Szemesi, Péter Bagi, Petra Nagy
Publikováno v:
The Journal of Organic Chemistry. 86:14493-14507
Secondary phosphine oxides incorporating various aryl and alkyl groups were synthesized in racemic form, and these products formed the library reported in this study. TADDOL derivatives were used to obtain the optical resolution of these P-stereogeni