메뉴 건너뛰기




Volumn 10, Issue 9, 1998, Pages 804-807

Influence of the nature and substitution of chiral 2,3-epoxy alcohol derivatives on the enantiomeric elution order on Chiralcel OD column

Author keywords

2,3 epoxyalcohols; Chain length influence; Enantiomeric elution order; Protective groups

Indexed keywords

ALCOHOL DERIVATIVE;

EID: 0031734134     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1520-636X(1998)10:9<804::AID-CHIR5>3.0.CO;2-O     Document Type: Article
Times cited : (5)

References (15)
  • 2
    • 2642642035 scopus 로고    scopus 로고
    • Recent advances on the chemoenzymatic synthesis of carbohydrates and carbohydrate mimetics
    • Gijsen, H.J.M., Qiao, L., Fitz, W., Wong, C.H. Recent advances on the chemoenzymatic synthesis of carbohydrates and carbohydrate mimetics. Chem. Rev. 96:443-473, 1996.
    • (1996) Chem. Rev. , vol.96 , pp. 443-473
    • Gijsen, H.J.M.1    Qiao, L.2    Fitz, W.3    Wong, C.H.4
  • 4
    • 0012815040 scopus 로고
    • The first practical method for asymmetric epoxidation
    • Tsutomu, T., Sharpless, K.B. The first practical method for asymmetric epoxidation. J. Am. Chem. Soc. 102:5974-5976, 1980.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 5974-5976
    • Tsutomu, T.1    Sharpless, K.B.2
  • 5
    • 0001533456 scopus 로고
    • The asymmetric epoxidation of divinyl carbinols: Theory and applications
    • Smith, D.B., Wang, Z., Schreiber, S.L. The asymmetric epoxidation of divinyl carbinols: Theory and applications. Tetrahedron 46:4793-4808, 1990.
    • (1990) Tetrahedron , vol.46 , pp. 4793-4808
    • Smith, D.B.1    Wang, Z.2    Schreiber, S.L.3
  • 6
    • 0000612931 scopus 로고
    • Synthesis of carbohydrates via tandem use of the osmium-catalyzed asymmetric dihydroxylation and enzyme-catalyzed aldol addition reactions
    • Henderson, I., Sharpless, K.B., Wong, C.-H. Synthesis of carbohydrates via tandem use of the osmium-catalyzed asymmetric dihydroxylation and enzyme-catalyzed aldol addition reactions. J. Am. Chem. Soc. 116:558-561, 1994.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 558-561
    • Henderson, I.1    Sharpless, K.B.2    Wong, C.-H.3
  • 8
    • 0028294668 scopus 로고
    • Contribution of preparative chromatographic resolution to the investigation of chiral phenomena
    • Francotte, E. Contribution of preparative chromatographic resolution to the investigation of chiral phenomena. J. Chromatogr. A 666:565-601, 1994.
    • (1994) J. Chromatogr. a , vol.666 , pp. 565-601
    • Francotte, E.1
  • 9
    • 0028946878 scopus 로고
    • Chiral high-performance liquid chromatography with cellulose carbamate-coated phases. Influence of support surface chemistry on enantioselectivity
    • Grieb, S.J., Matlin, SA, Belenguer, A.M., Ritchie, H.J. Chiral high-performance liquid chromatography with cellulose carbamate-coated phases. Influence of support surface chemistry on enantioselectivity. J. Chromatogr. A 697:271-278, 1995.
    • (1995) J. Chromatogr. a , vol.697 , pp. 271-278
    • Grieb, S.J.1    Matlin, S.A.2    Belenguer, A.M.3    Ritchie, H.J.4
  • 10
    • 0027263210 scopus 로고
    • Diastereoface differentiation in addition of lithium enolates to chiral α,β-epoxyaldehydes
    • Escudier, J.-M., Baltas, M., Gorrichon, L. Diastereoface differentiation in addition of lithium enolates to chiral α,β-epoxyaldehydes. Tetrahedron 49:5253-5266, 1993.
    • (1993) Tetrahedron , vol.49 , pp. 5253-5266
    • Escudier, J.-M.1    Baltas, M.2    Gorrichon, L.3
  • 11
    • 0030185484 scopus 로고    scopus 로고
    • Enhanced diastereoselectivity in the addition of ester enolate to optically active α,β-epoxyaldehydes obtained from nerol and geraniol
    • Nacro, K., Baltas, M., Escudier, J.-M., Gorrichon, L. Enhanced diastereoselectivity in the addition of ester enolate to optically active α,β-epoxyaldehydes obtained from nerol and geraniol. Tetrahedron 52: 9047-9056, 1996.
    • (1996) Tetrahedron , vol.52 , pp. 9047-9056
    • Nacro, K.1    Baltas, M.2    Escudier, J.-M.3    Gorrichon, L.4
  • 13
    • 0031012715 scopus 로고    scopus 로고
    • Stereoselective synthesis of five and/or six membered ring hydroxylactones obtained by Lewis acid mediated reaction of γ,δ-epoxy-β-hydroxyesters; access to 5-methylated 2-deoxysugars
    • Nacro, K., Baltas, M., Escudier, J.-M., Gorrichon, L. Stereoselective synthesis of five and/or six membered ring hydroxylactones obtained by Lewis acid mediated reaction of γ,δ-epoxy-β-hydroxyesters; access to 5-methylated 2-deoxysugars. Tetrahedron 53:659-672, 1997.
    • (1997) Tetrahedron , vol.53 , pp. 659-672
    • Nacro, K.1    Baltas, M.2    Escudier, J.-M.3    Gorrichon, L.4
  • 14
    • 0028868722 scopus 로고
    • Synthesis of a 3-deoxy-D-arabino-2-heptulosonic acid derivative
    • Devianne, G., Escudier, J.-M., Baltas, M., Gorrichon, L. Synthesis of a 3-deoxy-D-arabino-2-heptulosonic acid derivative. J. Org. Chem. 60: 7343-7347, 1995.
    • (1995) J. Org. Chem. , vol.60 , pp. 7343-7347
    • Devianne, G.1    Escudier, J.-M.2    Baltas, M.3    Gorrichon, L.4
  • 15
    • 0029879166 scopus 로고    scopus 로고
    • Diastereoselective synthesis of (1S,2S,3R,6S) 3-chloro-3-methyl-6-isopropenyl-1,2-cydohexanediol via Prins reaction induced by Zinc and trimethylsilyl chloride
    • Marty, M., Stoeckli-Evans, H., Neier, R. Diastereoselective synthesis of (1S,2S,3R,6S) 3-chloro-3-methyl-6-isopropenyl-1,2-cydohexanediol via Prins reaction induced by Zinc and trimethylsilyl chloride. Tetrahedron 52:4645-4658, 1996.
    • (1996) Tetrahedron , vol.52 , pp. 4645-4658
    • Marty, M.1    Stoeckli-Evans, H.2    Neier, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.