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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 77 (1994), S. 1520-1526 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclo(-D-Leu-L-MeLeu-D-Leu-L-MeLeu-D-Leu-L-MeLeu-) (1) and cyclo(-L-Leu-D-Leu-L-MeLeu-D-Leu-L-Leu-D-Leu-) (2) were synthesized and used for a study of the interaction of β -rings in solution. In appropriate solvents, 1 and 2 formed dimers consisting of two β -rings connected through six interannular H-bonds and having the N -Me group(s) on the solvent-exposed face. The study also afforded indications that 2 formed different dimers of this kind, differing in the relative orientation of the two β -rings. These experimental observations provide strong support to the idea that unsubstituted D,L-alternating cyclooligopeptides, such as cyclo(hexaleucine), can self-assemble and give rise to long tubular stacks of β -rings.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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