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Volumn , Issue 12, 1999, Pages 1981-1983

Kinetic enzymatic resolution of cyclopropane derivatives

Author keywords

Asymmetric synthesis; Boron; Cyclopropanes; Enantiomeric resolution; Enzymes

Indexed keywords

CYCLOPROPANE DERIVATIVE;

EID: 0032733359     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-2983     Document Type: Article
Times cited : (15)

References (41)
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    • (b) Schmid, R. D.; Verger, R. Angew. Chem. 1998, 110, 1694; Angew. Chem. Int. Ed. 1998, 37, 1608;
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1608
  • 15
    • 84920357932 scopus 로고
    • (g) Schneider, M.; Engel, N.; Hönicke, P.; Heinemann, G.; Görisch, H. Angew. Chem. 1984, 96, 55; Angew. Chem. Int. Ed. 1984, 23, 67;
    • (1984) Angew. Chem. Int. Ed. , vol.23 , pp. 67
  • 26
    • 0043117854 scopus 로고
    • The enantiomeric purity of the products was determined by glc using a Bondex β stationary phase: Fischer, P.; Aichholz, R.; Bölz, U.; Juzu, M.; Krimmer, S. Angew. Chem. 1990, 102, 439; Angew. Chem. Intl. Ed. Engl. 1990, 29, 427. Since in a kinetic resolution the enantiomeric excess of product and starting material varies as the reaction proceeds, it is more meaningful to use the E-value (enantiomeric ratio; measures the ability of the enzyme to distinguish between enantiomers) to compare reactions (see ref. 1, cit, ref.). A simple program to calculate the E-value for given enantiomeric ratios is available free of charge at http://www-orgc.tu-graz.ac.at: Kroutil, W.; Kleewein, A.; Faber, K. Tetrahedron: Asymmetry 1997, 8, 3251.
    • (1990) Angew. Chem. , vol.102 , pp. 439
    • Fischer, P.1    Aichholz, R.2    Bölz, U.3    Juzu, M.4    Krimmer, S.5
  • 27
    • 0025256980 scopus 로고
    • The enantiomeric purity of the products was determined by glc using a Bondex β stationary phase: Fischer, P.; Aichholz, R.; Bölz, U.; Juzu, M.; Krimmer, S. Angew. Chem. 1990, 102, 439; Angew. Chem. Intl. Ed. Engl. 1990, 29, 427. Since in a kinetic resolution the enantiomeric excess of product and starting material varies as the reaction proceeds, it is more meaningful to use the E-value (enantiomeric ratio; measures the ability of the enzyme to distinguish between enantiomers) to compare reactions (see ref. 1, cit, ref.). A simple program to calculate the E-value for given enantiomeric ratios is available free of charge at http://www-orgc.tu-graz.ac.at: Kroutil, W.; Kleewein, A.; Faber, K. Tetrahedron: Asymmetry 1997, 8, 3251.
    • (1990) Angew. Chem. Intl. Ed. Engl. , vol.29 , pp. 427
  • 28
    • 0030809631 scopus 로고    scopus 로고
    • The enantiomeric purity of the products was determined by glc using a Bondex β stationary phase: Fischer, P.; Aichholz, R.; Bölz, U.; Juzu, M.; Krimmer, S. Angew. Chem. 1990, 102, 439; Angew. Chem. Intl. Ed. Engl. 1990, 29, 427. Since in a kinetic resolution the enantiomeric excess of product and starting material varies as the reaction proceeds, it is more meaningful to use the E-value (enantiomeric ratio; measures the ability of the enzyme to distinguish between enantiomers) to compare reactions (see ref. 1, cit, ref.). A simple program to calculate the E-value for given enantiomeric ratios is available free of charge at http://www-orgc.tu-graz.ac.at: Kroutil, W.; Kleewein, A.; Faber, K. Tetrahedron: Asymmetry 1997, 8, 3251.
    • (1997) Tetrahedron: Asymmetry , vol.8 , pp. 3251
    • Kroutil, W.1    Kleewein, A.2    Faber, K.3
  • 40
    • 0003057996 scopus 로고    scopus 로고
    • Alternative synthesis of (3-phenylcyclopropyl)methanol (93% ee) using equimolar amounts of a chiral modifier: Charette, A. B.; Lebel, H. Org. Synth. 1998, 76, 86.
    • (1998) Org. Synth. , vol.76 , pp. 86
    • Charette, A.B.1    Lebel, H.2
  • 41
    • 84920346883 scopus 로고    scopus 로고
    • note
    • 12O (148.20): calcd. C 81.04, H 8.16; found C 81.03, H 8.21.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.