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  • Hydrolyses  (1)
  • amylose tris(3,5-dimethylphenylcarbamate)  (1)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 9 (1997), S. 727-731 
    ISSN: 0899-0042
    Keywords: chiral HPLC ; amylose tris(3,5-dimethylphenylcarbamate) ; cellulose tris(3,5-dimethylphenylcarbamate) ; cellulose tris(4-methylbenzoate) ; imine enantiomers ; e.e. determination ; imine isomerization reaction ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A high-performance liquid chromatographic method has been developed for the analysis of the intermediate imines and end products in an asymmetric isomerization route toward optically active amines. Separation of the imine enantiomers was performed on commercially available Chiralcel OD-H, Chiralcel OJ, and Chiralpak AD chiral stationary phases. All substituted imine enantiomers could be readily resolved with selectivities (α) higher than 1.10 using the Chiralpak AD column. By derivatization with ring-substituted benzaldehydes, aromatic amines were converted into Schiff base derivatives and the enantiopurity of these amines was determined. Chirality 9:727-731, 1997. © 1997 Wiley-Liss, Inc.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-193X
    Keywords: Enzymes ; Kinetic resolution ; Sulfoxides ; Chiral resolution ; Hydrolyses ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Selected racemic trans-2-alkoxycarbonyl-3,6-dihydro-2H-thiopyran S-oxides 2a-h have been subjected to enzyme-assisted hydrolysis under conditions of kinetic resolution to give the corresponding acids and recovered esters with moderate to high enantiomeric purities (up to 95%). The enantioselectivity of the reaction was found to be strongly dependent on the structures of the substrates used.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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