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  • 1
    ISSN: 1573-1111
    Keywords: Host synthesis ; crystalline inclusion compounds ; X-ray structure analysis ; 1,4-dioxane guest
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A novel host molecule, 1, suitable for crystalline lattice-type inclusion, has been synthesized, and its cocrystal formation ability has been investigated. Host 1 proved to be of potential use for organic solvent separation and retrieval, and a promising auxiliary for solidification of certain odorous substances. The crystal structures of the solvent-free host 1, and its complex with 1,4-dioxane (1 : 1), have been determined by single crystal X-ray diffraction. The structure of 1 (guest-free) is triclinic, P $${\bar 1}$$ , with a = 9.452(2), b = 10.359(3), c = 13.116(3) Å, α = 101.80(2), β = 106.53(1) and γ = 104.32(1)°. The spacious, propeller-like molecules are held together by weak van der Waals' forces. The dioxane inclusion compound is monoclinic, P21/a, with a = 15.050(1), b = 8.641(1) and c = 20.658(1) Å, and β = 94.56(1)°, and contains two crystallographically independent guest molecules, both located around symmetry centres. The molecular packing seems to be governed by C—H···O type bonds (C···O = 3.31 and 3.48 Å) from the host to the dioxane oxygens.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 5 (1993), S. 315-319 
    ISSN: 0899-0042
    Keywords: chiral selectors ; natural product derived hosts ; optically active hosts ; clathrate hosts ; bulky 1,2-diols ; inclusion compounds ; host-guest complexes ; chiroselective cocrystallization ; chiroselective vapor sorption ; preparative scale enantioseparation ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New optically active host compounds for chiroselective crystalline inclusion formation derived from natural lactic acid are synthesized. They enable useful enantiomer separations of different chiral compounds via cocrystallization and sorption on preparative scale including various ketones, lactones, alcohols, sulfoxides, and methyloxiranes. In the cases of 3-methylcyclohexanone, 4-methyl-δ-valerolactone, and 2-phenylpropanol, ees 〉 99% were obtained from one cocrystallization step using these hosts. © 1993 Wiley-Liss, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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