Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Harri Czesla"'
Autor:
Maximilian Kühnle, Volker Schurig, Diana Kreidler, Paul Schuler, Harri Czesla, Karsten Holtin, Klaus Albert
Publikováno v:
Chirality. 22:808-812
The hyphenation of enantioselective capillary gas chromatography and mass spectrometry is not always sufficient to distinguish between structural isomers, thus requiring peak identification by NMR spectroscopy. Here the first online coupling of enant
Autor:
Klaus Albert, Andrew Webb, Diana Kreidler, Paul Schuler, Volker Schurig, Harri Czesla, Armin Purea, Marc David Grynbaum, Walter Schaal, Jens Rehbein
Publikováno v:
Analytical Chemistry. 79:2708-2713
Whereas the hyphenation of gas chromatography (GC) with mass spectrometry is of great importance, little is known about the coupling to nuclear magnetic resonance spectroscopy (NMR). The investigation of this technique is an attractive proposition be
Publikováno v:
Tetrahedron. 55:9787-9792
An improved synthesis of enantiomerically pure(S, E)-(+)-5-methylhept-2-en-4-one from(S)-(+)-2-methyl-1-butanol in four steps is reported. An improved chiral-pool synthesis of enantiomerically pure(S)-(+)-filbertone, starting from(S)-(+)-2-methyl-1-b
Publikováno v:
Journal of Microcolumn Separations. 9:421-431
The feasibility of miniaturized enantiomer separation by open tubular liquid chromatography (OTLC) as well as by open tubular electrochromatography (OTEC) in 50 μm i.d. and 25 μm i.d. fused silica capillaries coated with CHIRASIL-DEX, a covalently
Publikováno v:
ChemInform. 30
An improved synthesis of enantiomerically pure(S, E)-(+)-5-methylhept-2-en-4-one from(S)-(+)-2-methyl-1-butanol in four steps is reported. An improved chiral-pool synthesis of enantiomerically pure(S)-(+)-filbertone, starting from(S)-(+)-2-methyl-1-b
Publikováno v:
Chirality. 21(1)
The chromatographic enantioseparation of small unfunctionalized chiral alkanes C*HR(1)R(2)R(3) (R = alkyl) represents a challenge in separation science. Because of the lack of any functional groups, enantiorecognition in the presence of a chiral sele
Autor:
Klaus Albert, Karsten Holtin, Maximilian Kühnle, Paul Schuler, Diana Kreidler, Harri Czesla, Walter Schaal, Volker Schurig
Publikováno v:
Analytical chemistry. 80(14)
The identification of volatile cis/trans-stereoisomers was accomplished by employing a hyphenated GC-NMR system. The chromatographic and spectroscopic conditions were optimized with respect to the (1)H NMR detection. A special processing technique wa
Publikováno v:
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 875(1)
In an effort to simultaneously enantioseparate racemic unfunctionalized alkanes and racemic α-amino acid derivatives by gas chromatography (GC) in forthcoming experiments related to the search for extraterrestrial homochirality, the two versatile mo
Publikováno v:
Analytical chemistry. 79(12)
Inversion of the elution order of enantiomers caused by enthalpy-entropy compensation at the isoenantioselective temperature (Tiso) was experimentally observed by gas chromatography on the diamide-type chiral stationary phase (CSP), Chirasil-L-Val-C1
Publikováno v:
Journal of separation science. 30(1)
Combination of the enantioselective properties of the two versatile gas-chromatographic chiral stationary phases (CSPs) octakis(3-O-butanoyl-2,6-di-O-n-pentyl)-gamma-CD (Lipodex E) 1 and L-valine-diamide-based CSP Chirasil-Val-C11 2 has been realized