메뉴 건너뛰기




Volumn 39, Issue 2, 2010, Pages 549-554

Application of (S)-N-(4-Nitrophenoxycarbonyl) phenylalanine methoxyethyl ester as a chiral derivatizing reagent for reversed-phase high-performance liquid chromatographic separation of diastereomers of amino alcohols, non-protein amino acids, and PenA

Author keywords

(S) N (4 Nitrophenoxycarbonyl) phenylalanine methoxyethyl ester; Amino acids; Amino alcohols; Chiral separation; Diastereomers; DL PenA; HPLC

Indexed keywords

AMINO ACID; AMINOALCOHOL; N (4 NITROPHENOXYCARBONYL)PHENYLALANINE METHOXYETHYL ESTER; PENICILLAMINE; REAGENT; UNCLASSIFIED DRUG; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; N-(4-NITROPHENOXYCARBONYL)PHENYLALANINE METHOXYETHYL ESTER; NITRO DERIVATIVE;

EID: 84755161467     PISSN: 09394451     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00726-010-0472-z     Document Type: Article
Times cited : (10)

References (15)
  • 1
    • 3943090437 scopus 로고    scopus 로고
    • High-performance liquid chromatographic separation of stereoisomers of ß-amino acids and a comparison of separation efficiencies on chirobiotic T and TAG columns
    • Årki A, Tourwé D, Solymár M, Fülöp F, Armstrong DW, Péter A (2004) High-performance liquid chromatographic separation of stereoisomers of ß-amino acids and a comparison of separation efficiencies on chirobiotic T and TAG columns. Chromatographia 60: S43-S54
    • (2004) Chromatographia , vol.60
    • Årki, A.1    Tourwé, D.2    Solymár, M.3    Fülöp, F.4    Armstrong, D.W.5    Péter, A.6
  • 2
    • 46449109624 scopus 로고    scopus 로고
    • Indirect enantioseparation of α-amino acids by reversed-phase liquid chromatography using new chiral derivatizing reagents synthesized from s-triazine chloride
    • Bhushan R, Kumar V (2008a) Indirect enantioseparation of α-amino acids by reversed-phase liquid chromatography using new chiral derivatizing reagents synthesized from s-triazine chloride. J Chromatogr A 1201:35-42
    • (2008) J. Chromatogr. A , vol.1201 , pp. 35-42
    • Bhushan, R.1    Kumar, V.2
  • 3
    • 60649115660 scopus 로고    scopus 로고
    • Synthesis and application of new chiral variants of Marfey's reagent for liquid chromatographic separation of the enantiomers of α-amino acids
    • Bhushan R, Kumar V (2008b) Synthesis and application of new chiral variants of Marfey's reagent for liquid chromatographic separation of the enantiomers of α-amino acids. Acta Chromatogr 20:329-347
    • (2008) Acta Chromatogr. , vol.20 , pp. 329-347
    • Bhushan, R.1    Kumar, V.2
  • 4
    • 75149131596 scopus 로고    scopus 로고
    • Enantioresolution of DL-penicillamine
    • doi:10.1002/bmc.1355
    • Bhushan R, Kumar R (2010) Enantioresolution of DL-penicillamine. Biomed Chromatogr 24:66-92. doi:10.1002/bmc.1355
    • (2010) Biomed. Chromatogr. , vol.24 , pp. 66-92
    • Bhushan, R.1    Kumar, R.2
  • 5
    • 34848897455 scopus 로고    scopus 로고
    • Indirect resolution of enantiomers of penicillamine by TLC and HPLC using Marfey's reagent and its variants
    • DOI 10.1002/bmc.854
    • Bhushan R, Brückner H, Kumar V (2007) Indirect resolution of enantiomers of penicillamine by TLC and HPLC using Marfey's reagent and its variants. Biomed Chromatogr 21:1064-1068 (Pubitemid 47495629)
    • (2007) Biomedical Chromatography , vol.21 , Issue.10 , pp. 1064-1068
    • Bhushan, R.1    Bruckner, H.2    Kumar, V.3
  • 6
    • 67349118456 scopus 로고    scopus 로고
    • Chromatographic separation of enantiomers of non-protein α-amino acids after derivatization with Marfey's reagent and its four variants
    • doi:10.1007/s00726-008-0135-5
    • Bhushan R, Kumar V, Tanwar S (2009) Chromatographic separation of enantiomers of non-protein α-amino acids after derivatization with Marfey's reagent and its four variants. Amino Acids 36:571-579. doi:10.1007/s00726-008-0135-5
    • (2009) Amino Acids , vol.36 , pp. 571-579
    • Bhushan, R.1    Kumar, V.2    Tanwar, S.3
  • 7
    • 0030875121 scopus 로고    scopus 로고
    • A nonempirical method using LC/MS for determination of the absolute configuration of constituent amino acids in a peptide: Elucidation of limitations of Marfey's method and of its separation mechanism
    • Fujii K, Ikai Y, Mayumi T, Oka H, Suzuki M, Harada K (1997) A nonempirical method using LC/MS for determination of the absolute configuration of constituent amino acids in a peptide: elucidation of limitations of Marfey's method and of its separation mechanism. Anal Chem 69:3346-3352
    • (1997) Anal. Chem. , vol.69 , pp. 3346-3352
    • Fujii, K.1    Ikai, Y.2    Mayumi, T.3    Oka, H.4    Suzuki, M.5    Harada, K.6
  • 8
    • 1842532624 scopus 로고    scopus 로고
    • Chirality determination of unusual amino acids using precolumn derivatization and liquid chromatographyelectrospray ionization mass spectrometry
    • Hess S, Gustafson KR, Milanowski DJ, Alvira E, Lipton MA, Pannell LK (2004) Chirality determination of unusual amino acids using precolumn derivatization and liquid chromatographyelectrospray ionization mass spectrometry. J Chromatogr A 1035:211-219
    • (2004) J. Chromatogr. A , vol.1035 , pp. 211-219
    • Hess, S.1    Gustafson, K.R.2    Milanowski, D.J.3    Alvira, E.4    Lipton, M.A.5    Pannell, L.K.6
  • 9
    • 0027051353 scopus 로고
    • Resolution of the enantiomers of thiol compounds by reversed-phase liquid chromatography using chiral derivatization with 2, 3, 4, 6-tetra-O-acetyl- β-D-glucopyranosylisothiocyanate
    • Ito S, Ota A, Yamamoto K, Kawashima Y (1992) Resolution of the enantiomers of thiol compounds by reversed-phase liquid chromatography using chiral derivatization with 2, 3, 4, 6-tetra-O-acetyl-β-D- glucopyranosylisothiocyanate. J Chromatogr 626:187-196
    • (1992) J. Chromatogr. , vol.626 , pp. 187-196
    • Ito, S.1    Ota, A.2    Yamamoto, K.3    Kawashima, Y.4
  • 10
    • 0031841520 scopus 로고    scopus 로고
    • Indirect resolution of thiol enantiomers by high-performance liquid chromatography with a fluorescent chiral tagging reagent
    • Jin D, Toyo'oka T (1998) Indirect resolution of thiol enantiomers by high-performance liquid chromatography with a fluorescent chiral tagging reagent. Analyst 123:1271-1277
    • (1998) Analyst , vol.123 , pp. 1271-1277
    • Jin, D.1    Toyo'oka, T.2
  • 11
    • 0034960071 scopus 로고    scopus 로고
    • HPLC enantioseparation of phenylalanine analogs by application of (S)-N-(4-nitrophenoxycarbonyl) phenylalanine methoxyethyl ester as a new chiral derivatizing agent
    • Olajos E, Péter A, Casimir R, Tourwé D (2001) HPLC enantioseparation of phenylalanine analogs by application of (S)-N-(4-nitrophenoxycarbonyl) phenylalanine methoxyethyl ester as a new chiral derivatizing agent. Chromatographia 54:77-82
    • (2001) Chromatographia , vol.54 , pp. 77-82
    • Olajos, E.1    Péter, A.2    Casimir, R.3    Tourwé, D.4
  • 12
    • 0034523937 scopus 로고    scopus 로고
    • Application of (S)-N-(4-nitrophenoxycarbonyl) phenylalanine methoxyethyl ester as a new chiral derivatizing agent for proteinogenic amino acid analysis by high performance liquid chromatography
    • Péter A, Vékes E, Torok G (2000) Application of (S)-N-(4-nitrophenoxycarbonyl) phenylalanine methoxyethyl ester as a new chiral derivatizing agent for proteinogenic amino acid analysis by high performance liquid chromatography. Chromatographia 52:821-826
    • (2000) Chromatographia , vol.52 , pp. 821-826
    • Péter, A.1    Vékes, E.2    Torok, G.3
  • 13
    • 0036499918 scopus 로고    scopus 로고
    • Application of a new chiral derivatizing agent to the enantioseparation of secondary amino acids
    • Péter A, Vékes E, Toth G, Tourwé D, Borremans F (2002) Application of a new chiral derivatizing agent to the enantioseparation of secondary amino acids. J Chromatogr A 948:283-294
    • (2002) J. Chromatogr. A , vol.948 , pp. 283-294
    • Péter, A.1    Vékes, E.2    Toth, G.3    Tourwé, D.4    Borremans, F.5
  • 15
    • 0037040576 scopus 로고    scopus 로고
    • Indirect highperformance liquid chromatographic separation of stereoisomers of β-alkyl-substituted amino acids by the application of (S)-N-(4-nitrophenoxycarbonyl) phenylalanine methoxyethyl ester as chiral derivatizing agent
    • Vékes E, Torok G, Péter A, Sapi J, Tourwé D (2002) Indirect highperformance liquid chromatographic separation of stereoisomers of β-alkyl-substituted amino acids by the application of (S)-N-(4- nitrophenoxycarbonyl) phenylalanine methoxyethyl ester as chiral derivatizing agent. J Chromatogr A 949:125-139
    • (2002) J. Chromatogr. A , vol.949 , pp. 125-139
    • Vékes, E.1    Torok, G.2    Péter, A.3    Sapi, J.4    Tourwé, D.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.