Library

Language
Preferred search index
Number of Hits per Page
Default Sort Criterion
Default Sort Ordering
Size of Search History
Default Email Address
Default Export Format
Default Export Encoding
Facet list arrangement
Maximum number of values per filter
Auto Completion
Feed Format
Maximum Number of Items per Feed
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 22 (1983), S. 163-169 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Conformational studies on poly(oxyethylene)-bound homo-, oligo-, guest-host, and sequential peptides synthesized according to the liquid-phase method were carried out by means of 1H-nmr spectroscopy. The solubilizing effect of the C-terminal polymeric support allowed a thorough investigation of the secondary structure in solution.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 68 (1985), S. 705-714 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformational behavior of POE-bound model peptides Boc-(L-Ala)2-X-Y-(L-Ala)2-NHPOE (X - Y = L-Pro-Gly (I), Gly-L-Ile (II); NHPOE = aminopoly(oxyethylene)) as well as of the repetitive hexapeptide of elastin, Boc-L-Val-L-Ala-L-Pro-Gly-L-Val-Gly-A-NHPOE-M (III) (A = photosensitive 3-nitro-4-(bromomethyl)benzoyl group; NHPOE-M = aminopoly(oxyethylane) monomethyl ether) has been studied by means of 1H-NMR and CD spectroscopy. Compounds I and III form a β-turn with Pro and Gly in positions i + 1 and i + 2, respectively, while an aggregated state for II, has been identified. The results are in good agreement with published prediction codes giving experimental evidence for the dominance of short-range interactions to establish secondary structure in solution.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...