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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 5 (1993), S. 168-172 
    ISSN: 0899-0042
    Keywords: chiral stationary phase ; chiral 2-oxetanone ; TLC ; SFC ; preparative LC ; push-pull chromatography ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chiral β-lactones offer an easy and economic approach to novel chiral R- or S-configurated LC phases. The preferred method for their preparation is based on conventional ready-to-use aminopropyl-functionalized silicas, e.g., aminopropyl HPLC columns. The new stationary phases can be used for analytical and preparative separations and are particularly suitable for the resolution of rotatory and heterocyclic stereoisomers. Applications in the LC, SFC, and TLC mode are possible, including the use of β-lactone-based mobile phase additives in a “push-pull” combination. A large variety of organic solvents can be used as eluents. © 1993 Wiley-Liss, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Enantiomers of various chiral five- and six-membered-ring lactones, Which are important classes of compounds (flavour and Pheromone components, key intermediates in the synthesis of biologically active substances) have been separated chromatographically on the chiral phase cellulose triacetate, crystallographic form I (CTAI). For different series of five-membered-ring lactones, relationships have been found between the elution order of the enantiomers and their absolute configuration. Preparative resolutions of γ-Phenyl-γ-butyrolactone (1) and of the Pheromone component 5b have been carried out to demonstrate the applicability of the method to g-scale separations.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polymerizable N2-(4-chloro-2-methylphenyl)-N1-methylformamidine derivatives of (N-demethyl-chlordimeform) (2) were prepared, bearing either 4-vinylbenzyloxy- or 2-methacryloyloxyethoxycarbamoyl groups (5 and 7), and in addition, a triazatriphosphorine derivartive of 2 (8). The carbamoyl groups and the P-N linkages in the monomers, respectively, were specifically designed to release the insecticide 2 under the particular microenvironmental conditions on cotton leaves by hydrolytic cleaveage, triggered by the pH 8-10 of the leaf surface. Biossaying experiments using larvae of the Egyptian Cotton Leafworm (Spodoptera littoralis) on cotton plants confirmed methacrylate 7 as the only compound with sufficient bioactivity. Corresponding homo- and copolymers of 7, containing covalently bound pendent moieties of 2, showed advantageous physiochemical properties with regard to improved efficiency and reduced environmental and handling risks in conventional foliar applications. The biological data suggest that the release rates of the active agent from the polymers vary significantly, depending on the hydrophilicity of the comonomers and the type of formulation used.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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