Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Elfriede Zarbl"'
Autor:
Frank Wuggenig, Wolfgang Lindner, Elfriede Zarbl, Biljana Peric Simov, Friedrich Hammerschmidt, Michael Lämmerhofer
Publikováno v:
European Journal of Organic Chemistry. 2002:1139-1142
Treatment of the culture broth of fosfomycin (1) producing Streptomyces fradae with ammonia gives 2−3% of the C-1 epimeric compound 5, as well as the known (1R,2R)-2-amino-1-hydroxypropylphosphonic acid (3) derived from fosfomycin. The configuratio
Publikováno v:
Journal of Separation Science. 24:706-716
This study evaluates how enantioselectivity values for the separation of chiral N-derivatized amino acids achieved in non-aqueous ion-pair CE with cinchona alkaloid derived chiral counter-ions are related quantitatively to those obtained in enantiose
Publikováno v:
Journal of Chromatography A. 892:509-521
The potential of tert.-butylcarbamoylquinine as chiral selector (SO) added to a non-aqueous background electrolyte for the capillary electrophoretic separation of the enantiomers of N-derivatized amino acids (selectands, SAs) is evaluated. Separation
Publikováno v:
Tetrahedron: Asymmetry. 11:2955-2964
Diisopropyl 2-azido-1-acetoxyethylphosphonate (±)- 7 was hydrolysed with high enantioselectivity by lipase SP 524 to give α-hydroxyphosphonate ( S )-(−)- 6 and ester ( R )-(−)- 7 , which was saponified to give ( R )-(+)- 6 . The two α-hydroxyp
Autor:
Michael Lämmerhofer, Ernst Tobler, Frantisek Svec, Jean M. J. Fréchet, Elfriede Zarbl, Wolfgang Lindner
Publikováno v:
Electrophoresis. 24(17)
A new chiral monomer derived from cinchona alkaloid, namely O-9-(tert-butylcarbamoyl)-11-[2-(methacryloyloxy)ethylthio]-10,11-dihydroquinine 1, was employed for the preparation of enantioselective monolithic capillary columns by an in situ copolymeri
Autor:
Guiseppe Cannazza, Carlo Parenti, Wolfgang Lindner, Anna Woschek, Friedrich Hammerschmidt, Michael Lämmerhofer, Elfriede Zarbl
Novel enantioselective silica-supported strong and weak cation exchange (SCX and WCX) materials (3.5 μm particles) based on enantiomerically pure N-(4-allyloxy-3,5-dichlorobenzoyl)-2-amino-3,3-dimethylbutanesulfonic acid and corresponding phosphonic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c06c81d5c72752ef68da67ba12ca100
https://hdl.handle.net/11380/583847
https://hdl.handle.net/11380/583847
Publikováno v:
Electrophoresis. 22(15)
A stereoselective ion-pair nonaqueous capillary electrophoresis (NACE) method employing the partial filling technique with N-derivatized amino acids, e.g., (R)- and (S)-3,5-dinitrobenzoyl-leucine (DNB-Leu), as chiral selector for the separation of "p
Autor:
Wolfgang Lindner, Biljana Peric Simov, Michael Lämmerhofer, Elfriede Zarbl, Friedrich Hammerschmidt
Publikováno v:
Electrophoresis. 22(6)
A stereoselective nonaqueous capillary electrophoresis (CE) method utilizing O-(tert-butylcarbamoyl) quinine as chiral ion-pair agent and additive to the non aqueous background electrolyte was evaluated for the simultaneous separation of the enantiom
Publikováno v:
Electrophoresis; May2003, Vol. 24 Issue 10, p1668-1679, 12p