메뉴 건너뛰기




Volumn 17, Issue 2, 2005, Pages 79-84

Investigation of a tartaric acid-based linear polyamide and dimer as chiral selectors in liquid chromatography

Author keywords

Branched selector; CD spectroscopy; Chiral chromatography; Enantioselective chromatography; Poly(tartaramide); Twin selector

Indexed keywords

2 (1 PENTENOYLOXY) 1,3 BIS [(O,0' DIMETHYLBENZOYL) N PROPYLTARTARDIAMIDE]PROPANE; DIMER; POLYAMIDE; POLYMER; SOLVENT; SORBENT; TARTARIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 13244277950     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/chir.20106     Document Type: Article
Times cited : (12)

References (15)
  • 1
    • 0242385355 scopus 로고    scopus 로고
    • Effects from hydrogen bonding and rigidity on selectivity in tartaric acid-based chiral selectors for enantioselective liquid chromatography
    • Oxelbark J, Seile′n I. Effects from hydrogen bonding and rigidity on selectivity in tartaric acid-based chiral selectors for enantioselective liquid chromatography. Chirality 2003;15(9):787-793.
    • (2003) Chirality , vol.15 , Issue.9 , pp. 787-793
    • Oxelbark, J.1    Seilen, I.2
  • 2
    • 0033968930 scopus 로고    scopus 로고
    • Novel cinchona alkaloid carbamate C-9-dimers as chiral anion-exchange type selectors for high-performance liquid chromatography
    • Franco P, Lämmerhofer M, Klaus P, Lindner W. Novel cinchona alkaloid carbamate C-9-dimers as chiral anion-exchange type selectors for high-performance liquid chromatography. J Chromatogr A 2000;869:111-127.
    • (2000) J Chromatogr A , vol.869 , pp. 111-127
    • Franco, P.1    Lämmerhofer, M.2    Klaus, P.3    Lindner, W.4
  • 3
    • 0035979707 scopus 로고    scopus 로고
    • Preparation of highly selective stationary phases of high-performance liquid chromatographic separation of enantiomers by direct copolymerization of monomers with single or twin chiral ligands
    • Xu M, Brahmachary E, Janco M, Ling F, Svec F, Frechét J. Preparation of highly selective stationary phases of high-performance liquid chromatographic separation of enantiomers by direct copolymerization of monomers with single or twin chiral ligands. J Chromatogr A 2001;928:25-40.
    • (2001) J Chromatogr A , vol.928 , pp. 25-40
    • Xu, M.1    Brahmachary, E.2    Janco, M.3    Ling, F.4    Svec, F.5    Frechét, J.6
  • 4
    • 0000161283 scopus 로고    scopus 로고
    • Use of branched aliphatic linkers for the preparation of selective chiral media for the HPLC separation of enantiomers
    • Liu Y, Juneau K, Svec F, Frechét F. Use of branched aliphatic linkers for the preparation of selective chiral media for the HPLC separation of enantiomers. Polym Bull 1998;41:183-189.
    • (1998) Polym Bull , vol.41 , pp. 183-189
    • Liu, Y.1    Juneau, K.2    Svec, F.3    Frechét, F.4
  • 5
    • 0001228455 scopus 로고
    • Use of branched aliphatic linkers for the preparation of selective chiral media for the HPLC separation of enantiomers
    • Oi N, Nagase M, Sawada Y. Use of branched aliphatic linkers for the preparation of selective chiral media for the HPLC separation of enantiomers. J Chromatogr 1984;292:427-431.
    • (1984) J Chromatogr , vol.292 , pp. 427-431
    • Oi, N.1    Nagase, M.2    Sawada, Y.3
  • 6
    • 0034807112 scopus 로고    scopus 로고
    • S-Leucine and [(S)-1-(1-naphthyl)-ethyl]amine as chiral building blocks for a bifunctional system-synthesis of a new chiral stationary phase and evaluation of its biselector properties in the HPLC resolution of racemic compound
    • and references therein contain examples of two connected dissimilar selectors
    • Iuliano A, Attolino E, Salvadori P. (S)-Leucine and [(S)-1-(1-naphthyl)- ethyl]amine as chiral building blocks for a bifunctional system-synthesis of a new chiral stationary phase and evaluation of its biselector properties in the HPLC resolution of racemic compound. Eur J Org Chem 2001;3523-3529 and references therein contain examples of two connected dissimilar selectors.
    • (2001) Eur J Org Chem , pp. 3523-3529
    • Iuliano, A.1    Attolino, E.2    Salvadori, P.3
  • 7
    • 0037183413 scopus 로고    scopus 로고
    • Biselector enantioselective stationary phases for HPLC: Dependence of the chiral discrimination properties on stereochemistry and chemical nature of each unit of the chiral auxiliary
    • Iuliano A, Attolino E, Salvadori P. Biselector enantioselective stationary phases for HPLC: dependence of the chiral discrimination properties on stereochemistry and chemical nature of each unit of the chiral auxiliary. Tetrahedron: Asymm 2002;13(16):1805-1815.
    • (2002) Tetrahedron: Asymm , vol.13 , Issue.16 , pp. 1805-1815
    • Iuliano, A.1    Attolino, E.2    Salvadori, P.3
  • 8
    • 0032496122 scopus 로고    scopus 로고
    • Recent developments in asymmetric catalysis using synthetic polymers with main chain chirality
    • Pu L. Recent developments in asymmetric catalysis using synthetic polymers with main chain chirality. Tetrahedron: Asymm 1998;9:1457-1477.
    • (1998) Tetrahedron: Asymm , vol.9 , pp. 1457-1477
    • Pu, L.1
  • 9
    • 0035847276 scopus 로고    scopus 로고
    • Optically active synthetic polymers as chiral stationary phases in HPLC
    • Nakano T. Optically active synthetic polymers as chiral stationary phases in HPLC. J Chromatogr A 2001;906:205-225.
    • (2001) J Chromatogr A , vol.906 , pp. 205-225
    • Nakano, T.1
  • 10
    • 0037131661 scopus 로고    scopus 로고
    • A comparison of silica and porous graphitic carbon as support materials for a chiral selector in HPLC
    • Oxelbark J, Claeson S. A comparison of silica and porous graphitic carbon as support materials for a chiral selector in HPLC. Tetrahedron: Asymm 2002;13:2235-2240.
    • (2002) Tetrahedron: Asymm , vol.13 , pp. 2235-2240
    • Oxelbark, J.1    Claeson, S.2
  • 11
    • 0027678632 scopus 로고
    • Optically active polyamides derived from L-tartaric acid
    • Bou JJ, Rodriguez-Galan A, Munoz-Guerra S. Optically active polyamides derived from L-tartaric acid. Macromolecules 1993;26: 5664-5670.
    • (1993) Macromolecules , vol.26 , pp. 5664-5670
    • Bou, J.J.1    Rodriguez-Galan, A.2    Munoz-Guerra, S.3
  • 12
    • 0028847071 scopus 로고
    • A new class of network-polymeric chiral stationary phases
    • Allenmark S, Andersson S, Möller P, Sanchez D. A new class of network-polymeric chiral stationary phases. Chirality 1995;7:248-256.
    • (1995) Chirality , vol.7 , pp. 248-256
    • Allenmark, S.1    Andersson, S.2    Möller, P.3    Sanchez, D.4
  • 13
    • 0037277068 scopus 로고    scopus 로고
    • Evaluation of a chiral stationary phase derived from a simple Diels-Alder reaction
    • Thunberg L, Allenmark S. Evaluation of a chiral stationary phase derived from a simple Diels-Alder reaction. Chirality 2003;15:400-408.
    • (2003) Chirality , vol.15 , pp. 400-408
    • Thunberg, L.1    Allenmark, S.2
  • 14
    • 0023983338 scopus 로고
    • Synthesis of aromatic polyamides N,N′-bis(trimethylsilyl)- substituted aromatic diamines and aromatic diacid chlorides
    • Oishi Y, Kakimoto Y, Imai Y. Synthesis of aromatic polyamides N,N′-bis(trimethylsilyl)-substituted aromatic diamines and aromatic diacid chlorides. Macromolecules 1988;21:547.
    • (1988) Macromolecules , vol.21 , pp. 547
    • Oishi, Y.1    Kakimoto, Y.2    Imai, Y.3
  • 15
    • 0026851203 scopus 로고
    • Stereoregular polyamides derived from methylene-L-tartaric acid and aliphatic diamines
    • Rodriguez-Galan A, Bou JJ, Munoz-Guerra S. Stereoregular polyamides derived from methylene-L-tartaric acid and aliphatic diamines. J Polym Sci Part A: Polym Chem 1992;30:713-721.
    • (1992) J Polym Sci Part A: Polym Chem , vol.30 , pp. 713-721
    • Rodriguez-Galan, A.1    Bou, J.J.2    Munoz-Guerra, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.