Synthesis and characterization of chiral stationary phases from amino acids and small peptides for liquid chromatography fractionations of a racemic alcohol

[1]  K. Channabasavaiah,et al.  Synthesis of the pentadecapeptide sequence of the active site of rabbit muscle triosephosphate isomerase. , 2009, International journal of peptide and protein research.

[2]  S. Hara,et al.  Enantioselectivity of hydrogen-bond association in liquid-solid chromatography , 1986 .

[3]  D. A. Nelson,et al.  Characterization of a chiral tripeptide stationary phase for the liquid chromatographic separation of chiral dipeptides , 1985 .

[4]  D. Armstrong Chiral Stationary Phases for High Performance Liquid Chromatographic Separation of Enantiomers: A Mini-Review , 1984 .

[5]  C. Welch,et al.  Chromatographic separation of the enantiomers of acylated amines on chiral stationary phases , 1984 .

[6]  S. Allenmark Recent advances in methods of direct optical resolution. , 1984, Journal of biochemical and biophysical methods.

[7]  C. C. Siemion Preparation of High Efficiency Columns for High Performance Liquid Chromatography , 1983 .

[8]  K. Unger,et al.  Chiral Silica Packings with L-Proline or L-Hydroxyproline Bonded via Alkyl or Alkylbenzyl Chains for the Separation of the Enantiomers of α-Amino Acids by HPLC , 1982 .

[9]  J. Finn,et al.  A widely useful chiral stationary phase for the high-performance liquid chromatography separation of enantiomers , 1981 .

[10]  J. Finn,et al.  Broad spectrum resolution of optical isomers using chiral high-performance liquid chromatographic bonded phases , 1980 .

[11]  E. Grushka,et al.  Effects of pH, ionic strength, and organic modifier on the chromatographic behavior of amino acids and peptides using a bonded peptide stationary phase , 1978 .

[12]  E. Grushka,et al.  High-pressure liquid chromatography of amino acids and dipeptides on a tripeptide bonded stationary phase. , 1977, Journal of chromatography.

[13]  W. König,et al.  Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid unter Zusatz von 1‐Hydroxy‐benzotriazolen , 1970 .

[14]  G. W. Anderson,et al.  The Use of Esters of N-Hydroxysuccinimide in Peptide Synthesis , 1964 .

[15]  P. Katsoyannis,et al.  Insulin Peptides. VI. The Synthesis of a Partially Protected Nonapeptide Corresponding to the First Nine Amino Acid Residues of the A-Chain of Insulin , 1963 .

[16]  T. Pochapsky,et al.  Chromatographic separation of the enantiomers of 2-carboalkoxyindolines and N-aryl-α-amino esters on chiral stationary phases derived from N-(3,5-dinitrobenzoyl)-α-amino acids , 1985 .

[17]  L. Rogers,et al.  Mixing considerations in the development of a gradient microbore high-performance liquid chromatographic system , 1984 .

[18]  M. Hyun,et al.  A rational approach to the design of highly effective chiral stationary phases for the liquid chromatographic separation of enantiomers. , 1984, Journal of pharmaceutical and biomedical analysis.

[19]  G. Blaschke Chromatographic Resolution of Racemates. New analytical methods (17) , 1980 .

[20]  R. Audebert Direct Resolution of Enantiomers in Column Liquid Chromatography , 1979 .

[21]  L. D. Galan,et al.  Preparation and Chromatographic Properties of Some Chemically Bonded Phases for Reversed-Phase Liquid Chromatography , 1978 .

[22]  Choh Hao Li,et al.  The Synthesis of L-Valyl-L-lysyl-L-valyl-L-tyrosyl-L-proline1 , 1963 .

[23]  R. Schwyzer,et al.  Über aktivierte Ester V. Verwendung der Cyanmethylester‐Methode zur Herstellung von (N‐Carbobenzoxy‐S‐benzyl‐L‐cysteinyl)‐L‐tyrosyl‐L‐isoleucin auf verschiedenen Wegen , 1955 .