Library

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
  • 1985-1989  (1)
  • 1975-1979  (1)
  • Chemistry  (2)
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 9 (1977), S. 322-324 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The carbon-13 n.m.r. spectra of several oxaziridines were measured. Aliphatic and aromatic ipso carbon atoms trans to the lone pair of nitrogen in oxaziridines were shifted upfield by c. 9 ppm, and 3.4 ppm, respectively, in comparison with isomers of inverted configuration. The results suggest that the nitrogen lone pair is partially responsible for the observed upfield shifts.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 25 (1987), S. 480-483 
    ISSN: 0749-1581
    Keywords: Configurations ; Conformations ; Imidates ; NOE ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new method for determining conformations and configurations of imidate esters was developed based on NOE difference spectra in CDCI3. As a test of the method, methyl N-methylacetimidate was determined to exist in the E configuration, ap conformation, in agreement with assignments by homoallylic coupling and dipole moment data. Methyl N-tert-butylformimidate, for which existing methods were not suitable, was also determined to exist as E-ap. Two methyl benzimidates were investigated, the N-methyl derivative 2, which was E-ap, and the N-tert-butyl derivative 6, which exhibited an unusually easy E/Z isomerization at room temperature (Tc = 24°C). At -58 °C, resolved spectra showed the E/Z isomers of 6 in a 40:60 ratio. From NOE data (E)-6 was determined to exist mostly as the ap conformer and (Z)-6 as the sp conformer. These results, in agreement with chemical shift data, can be interpreted in terms of the unusual steric requirements of the tert-butyl group.
    Additional Material: 1 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...