Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Bernadett Vas-Feldhoffer"'
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
Autor:
Miklos Nyerges, Angelika Thurner, Bernadett Vas-Feldhoffer, Tamás Holczbauer, Ferenc Faigl, Éva Bottka
Publikováno v:
ARKIVOC, Vol 2015, Iss 4, Pp 80-96 (2015)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ec1d03df6ce9574c4dd23654fbb1dea
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p009.023
https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p009.023
Autor:
Mátyás Czugler, Bernadett Vas-Feldhoffer, Veronika Kudar, Miklós Kubinyi, Krisztina Pál, Ferenc Faigl
Publikováno v:
Chirality. 21:905-910
Site selective mono- and dimetalation methods have been developed for the functionalization of 1-[(1,1′-biphenyl)-2-yl]-1H-pyrrole. Optical resolution of the prepared 1-[(3-carboxy-1,1′-biphenyl)-2-yl]pyrrole-2-carboxylic acid provided new atropi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73be6b18c3393f844849e7d63f7893e2
https://doi.org/10.1002/chir.20686
https://doi.org/10.1002/chir.20686
Autor:
Gábor Tárkányi, Mátyás Czugler, Bernadett Vas-Feldhoffer, Miklós Kubinyi, Ferenc Faigl, Krisztina Pál
Publikováno v:
Tetrahedron: Asymmetry. 20:98-103
An efficient synthesis and resolution of (±)-1-(2-carboxymethyl-6-ethylphenyl)- 1H -pyrrole-2-carboxylic acid has been developed for the preparation of novel optically active atropisomers. The ee values were measured by a 1 H NMR spectroscopic metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6229ed3ea965629673c2c978eb57459
https://doi.org/10.1016/j.tetasy.2009.01.010
https://doi.org/10.1016/j.tetasy.2009.01.010
Publikováno v:
ChemInform. 38
Novel regioselective methods have been developed for the mono‐ and difunctionalization of alkyl groups containing 1‐phenylpyrroles using different organometallic reagents. Tailoring the reagents and conditions allowed us to prepare several new mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::582543c76431b17d73bfd327f9b4a545
https://doi.org/10.1002/chin.200712115
https://doi.org/10.1002/chin.200712115