ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
Filter
Collection
Keywords
Publisher
Years
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1977 (1977), S. 709-726 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cyclic Cross-Conjugated Bond Systems, 30.  -  13C-Analyses of Methylenenorbornadiene DerivativesIn order to assess the homoconjugative relationship in the methylenenorbornadiene skeleton (3) the 13C-spectra of derivatives with alkyl-, aryl-, cyclopentadienylidene-, and cyano substituents in position 8 as well as with electron-withdrawing groups (CO2CH3, CN, CF3) on the endocyclic C=C-bonds have been analyzed. Comparison with saturated and cross-conjugated reference systems substantiates the low polarisability of the semicyclic C=C-bond in 3 and gives indications that increasing electron attraction in position 8 can intensify the homoconjugation, albeit only slightly.
    Notes: Zur Beurteilung der homokonjugativen Beziehung im Methylennorbornadien-Gerüst (3) werden die 13C-Spektren von Derivaten mit Alkyl-, Aryl-, Cyclopentadienyliden- und Cyanresten in Position 8 und zusätzlichen elektronenziehenden Resten (CO2CH3, CN, CF3) an den endocyclischen C=C-Bindungen analysiert. Der Vergleich mit verschiedenen gesättigten und gekreuzt-konjugierten Referenzsystemen belegt eine stark verringerte Polarisierbarkeit der semicyclischen C=C-Bindung in 3 und liefert Hinweise dafür, daß durch Verstärkung des Elektronenzugs in Position 8 die homokonjugative Wechselwirkung - wenn auch nur wenig - intensiviert werden kann.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...