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0344475592
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PCT Int. Appl. WO 97 11,070 (C1.C07D401/12), 27 Mar 1997, US Appl. 4, 193, 22 Sep 1995
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T. Belliotti, S. R. Kesten, T. A. Pugsley, D. J. Wustrow, Preparation of Heteroaryl-Substituted Cyclohexylamines as Central Nervous System (CNS) Agents, PCT Int. Appl. WO 97 11,070 (C1.C07D401/12), 27 Mar 1997, US Appl. 4, 193, 22 Sep 1995.
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Preparation of heteroaryl-substituted cyclohexylamines as central nervous system (CNS) agents
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Belliotti, T.1
Kesten, S.R.2
Pugsley, T.A.3
Wustrow, D.J.4
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2
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0012095530
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Determination of D-amino acids. I. Hydrolysis of DNP-L-amino acid methyl esters with carboxypeptidase-y
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P. Marfey, M. Ottesen, "Determination of D-Amino Acids. I. Hydrolysis of DNP-L-Amino Acid Methyl Esters with Carboxypeptidase-Y," Carlsberg Res. Comm., 49, 585-590 (1984).
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Marfey, P.1
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Determination of D-amino acids. II. Use of a bifunctional reagent, 1,5-difluoro-2,4-dinitrobenzene
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P. Marfey, "Determination of D-Amino Acids. II. Use of a Bifunctional Reagent, 1,5-Difluoro-2,4-Dinitrobenzene," Carlsberg Res. Comm., 49, 591-596 (1984).
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Marfey, P.1
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4
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Separation by high-performance liquid chromatography of (3R)-and (3S)-β-leucine as diastereomeric derivatives
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D. J. Aberhart, J. A. Getting, H. J. Lin, "Separation By High-Performance Liquid Chromatography of (3R)-And (3S)-β-Leucine as Diastereomeric Derivatives," Anal. Biochem., 151, 88-91 (1985).
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Aberhart, D.J.1
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Application of Marfey's reagent in racemization studies of amino acids and peptides
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G. Szokan, G. Mezo, F. Hudecz, "Application of Marfey's Reagent in Racemization Studies of Amino Acids and Peptides," J. Chromatogr., 444, 115-122 (1988).
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Szokan, G.1
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6
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0024459336
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Stereospecificity of reactions catalyzed by bacterial D-amino acid transaminase
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A. Martinez del Pozo, M. Merola, H. Ueno, J. M. Manning, K. Tanizawa, K. Nishimura, K. Soda, D. Ringe, "Stereospecificity of Reactions Catalyzed by Bacterial D-amino Acid Transaminase," J. Biol. Chem., 264, 17784-17789 (1989).
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Tanizawa, K.5
Nishimura, K.6
Soda, K.7
Ringe, D.8
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7
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0024747257
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Racemization analyses of peptides and amino acid derivatives by chromatography with pre-column derivatization
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G. Szokan, G. Mezo, F. Hudecz, Z. Majer, I. Schon, O. Nyeki, T. Szirtes, R. Dolling, "Racemization Analyses of Peptides and Amino Acid Derivatives by Chromatography with Pre-column Derivatization", J. Liquid Chromatogr., 12, 2855-2875 (1989).
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Schon, I.5
Nyeki, O.6
Szirtes, T.7
Dolling, R.8
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8
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0025864144
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High-performance liquid chromatographic separation of DL-amino acids derivatized with chiral variants of Sanger's reagent
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H. Bruckner, C. Gah, "High-performance Liquid Chromatographic Separation of DL-Amino Acids Derivatized with Chiral Variants of Sanger's Reagent", J. Chromatogr., 555, 81-95 (1991).
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9
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0345338311
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Validation of an enantioselective HPLC method for the determination of PD 144550 in CI-1008 drug substance
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internal communication.
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C. J. Calvitt, S. Priebe, G. Karrick, "Validation of An Enantioselective HPLC Method for the Determination of PD 144550 in CI-1008 Drug Substance," Parke-Davis Pharm. Res. Div., 1994, internal communication.
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Parke-Davis Pharm. Res. Div.
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Calvitt, C.J.1
Priebe, S.2
Karrick, G.3
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10
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0028170584
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HPLC determination of enantiomeric purity of protected amino acid derivatives used in peptide synthesis
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G. Szokan, S. Hadfi, K. Krizsan, A. Liembeck, I. Krecz, M. Almas, C. Somlai, "HPLC Determination of Enantiomeric Purity of Protected Amino Acid Derivatives used in Peptide Synthesis," J. Liq. Chromatogr., 17, 2759-2775 (1994).
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Szokan, G.1
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Liembeck, A.4
Krecz, I.5
Almas, M.6
Somlai, C.7
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11
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0028124327
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Enantiomeric derivatization for biomedical chromatography
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S. Gorog, M. Gazdag, "Enantiomeric Derivatization for Biomedical Chromatography," J. Chromatogr., B, 659, 51-84 (1994).
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J. Chromatogr.
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Gorog, S.1
Gazdag, M.2
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12
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0029122166
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Peptide chiral purity determination: Hydrolysis in deuterated acid, derivatization with Marfey's reagent and analysis using high-performance liquid chromatography-electrospray ionization-mass spectrometry
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D. R. Goodlett, P. A. Abuaf, P. A. Savage, K. A. Kowalski, T. K. Mukherjee, J. W. Tolan, N. Corkum, G. Goldstein, J. B. Crowther, "Peptide Chiral Purity Determination: Hydrolysis in Deuterated Acid, Derivatization with Marfey's Reagent and Analysis using High-performance Liquid Chromatography-Electrospray Ionization-Mass Spectrometry," J. Chromatogr., A, 707, 233-244 (1995).
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Goodlett, D.R.1
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Kowalski, K.A.4
Mukherjee, T.K.5
Tolan, J.W.6
Corkum, N.7
Goldstein, G.8
Crowther, J.B.9
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13
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0028860649
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High-performance liquid chromatographic method for the separation of isomers of cis-and trans-2-amino-cyclopentane-1-carboxylic acid
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A. Peter, F. Fulop, "High-performance Liquid Chromatographic Method for the Separation of Isomers of cis-and trans-2-Amino-cyclopentane-1-carboxylic Acid," J. Chromatogr., A, 715, 219-226 (1995).
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Peter, A.1
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14
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0039117872
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Separation of enantiomeric β-methyl amino acids and of β-methyl amino acid containing peptides
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A. Peter, G. Toth, G. Torok, D. Tourwe, "Separation of Enantiomeric β-Methyl Amino Acids and of β-Methyl Amino Acid containing Peptides," J. Chromatogr., A, 728, 455-465 (1996).
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Peter, A.1
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Tourwe, D.4
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15
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0028820805
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Separation and quantification of D-and L-phosphoserine in rat brain using Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide (Marfey's reagent) by high-performance liquid chromatography with ultraviolet detection
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D. B. Goodnough, M. P. Lutz, P. L. Wood, "Separation and Quantification of D-and L-Phosphoserine in Rat Brain using Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide (Marfey's Reagent) by High-performance Liquid Chromatography with Ultraviolet Detection," J. Chromatogr., B, 672, 290-294 (1995).
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Goodnough, D.B.1
Lutz, M.P.2
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16
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0031567013
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High-performance liquid chromatographic methods for separation of enantiomers of alicyclic β-amino acids
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A. Peter, G. Torok, P. Csomos, M. Peter, G. Bernath, F. Fulop, "High-performance Liquid Chromatographic Methods for Separation of Enantiomers of Alicyclic β-Amino Acids," J. Chromatogr., A, 761, 103-113 (1997).
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Peter, A.1
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Peter, M.4
Bernath, G.5
Fulop, F.6
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17
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0031447210
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High-performance liquid chromatographic separation of enantiomers of 1,1'-binaphthyl-substituted α-aminoisobutyric acid
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A. Peter, G. Torok, J. P. Mazaleyrat, M. Wakselman, "High-performance Liquid Chromatographic Separation of Enantiomers of 1,1'-Binaphthyl-substituted α-Aminoisobutyric Acid," J. Chromatogr., A, 790, 41-46 ( (1997).
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Peter, A.1
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18
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0032570994
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Chromatographic methods for monitoring the optical isomers of unusual aromatic amino acids
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A. Peter, G. Torok, G. Toth, W. V. D. Nest, G. Laus, D. Tourwe, "Chromatographic Methods for Monitoring the Optical Isomers of Unusual Aromatic Amino Acids," J. Chromatogr., A, 797, 165-176 (1998).
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19
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0032570958
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High-performance liquid chromatographic methods for separation of the isomers of β-amino acids possessing bicyclo[2.2.1]heptane or heptene skeletons
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G. Torok, A. Peter, P. Cosmos, L. T. Kanerva, F. Fulop, "High-performance Liquid Chromatographic Methods for Separation of the Isomers of β-Amino Acids Possessing Bicyclo[2.2.1]heptane or Heptene Skeletons," J. Chromatogr., A, 797, 177-186 (1998).
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Torok, G.1
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20
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0028064981
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Enantiomeric separation of amphetamine, methamphetamine and ring substituted amphetamines by means of a β-cyclodextrin-chiral stationary phase
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A. M. Rizzi, R. Hirz, S. Cladrowa-Runge, H. Jonsson, "Enantiomeric Separation of Amphetamine, Methamphetamine and Ring Substituted Amphetamines by Means of a β-Cyclodextrin-Chiral Stationary Phase," Chromatographia, 39, 131-137 (1994).
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Rizzi, A.M.1
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21
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0345338310
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4-Aminocyclohexylacetic acid and its ethyl ester were synthesized by Dr. Chemical Development Department, Parke-Davis Pharmaceutical Research Division, Holland, MI.
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4-Aminocyclohexylacetic acid and its ethyl ester were synthesized by Dr. Donald E. Butler and Mr. Tung Le, Chemical Development Department, Parke-Davis Pharmaceutical Research Division, Holland, MI.
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Butler, D.E.1
Tung, L.2
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