Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Laszlo Birincsik"'
Autor:
László Poppe, Gábor Seres, Antal Szabó, Balázs Erdélyi, József Ivanics, Laszlo Birincsik, Gábor Szatzker
Publikováno v:
Tetrahedron: Asymmetry. 17:268-274
Substituted ( S )-1-phenyl- 2a – h and ( S )-1-benzyl-propan-2-ols 4a and b , and ( S )-1-phenylethanol 6 were produced from prochiral ketones 1a – h , 3a , b and 5 by reductions with freshly harvested Zygosaccharomyces rouxii and Debaryomyces ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::378efa0f59d571710aa4d13e51bf8fd5
https://doi.org/10.1016/j.tetasy.2005.12.025
https://doi.org/10.1016/j.tetasy.2005.12.025
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 29:195-199
Talampanel is a non-competitive antagonist of AMPA receptor, and it is a drug studied for the treatment of epilepsy and cerebrovascular ischemia. The first step of an efficient synthesis of talampanel is the reduction of 3,4-methylenedioxyphenyl-acet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e954336c3f7a793feaab6a878b3182ee
https://doi.org/10.1016/j.molcatb.2003.10.015
https://doi.org/10.1016/j.molcatb.2003.10.015
Autor:
Balázs Erdélyi, Gábor Seres, Antal Szabó, Janos Salat, József Ivanics, Attila Konya, Laszlo Birincsik
Publikováno v:
Journal of Planar Chromatography – Modern TLC. 17:132-136
TLC methods have been developed for monitoring microbial enantioselective reduction and regioselective oxidation. The work discussed in this paper focused on preparation of aromatic chiral alcohols by bioreduction of their respective acetone derivati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbcef010e4c412c6a904200ecdfb335e
https://doi.org/10.1556/jpc.17.2004.2.9
https://doi.org/10.1556/jpc.17.2004.2.9
Publikováno v:
Journal of Planar Chromatography – Modern TLC. 16:246-248
A novel class of orally active 2,3-benzodiazepines has recently been discovered and patented by Hungarian researchers [1]. Biological activity studies led to the discovery of (8R)-7-acetyl5-(4-aminophenyl)-8,9-dihydro-8-methyl-7H-1,3-dioxolo[4,5h]-[2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbeaea36507ac7066e56d40410a5a3b4
https://doi.org/10.1556/jpc.16.2003.3.15
https://doi.org/10.1556/jpc.16.2003.3.15