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Kammermeier, T. ; Kaiser, A. ; Lee, G. S. ; Burgemeister, Thomas ; Wiegrebe, Wolfgang

Formation of 1H-Aziridines from Chalcones and Hydroxylamine

Kammermeier, T., Kaiser, A., Lee, G. S., Burgemeister, Thomas and Wiegrebe, Wolfgang (1994) Formation of 1H-Aziridines from Chalcones and Hydroxylamine. Archiv der Pharmazie 327, pp. 207-210.

Date of publication of this fulltext: 12 Jul 2010 09:40
Article
DOI to cite this document: 10.5283/epub.15793


Abstract

Highly substituted chalcones 1 do not react with two molecules of hydroxylamine affording dioximes 2 or hydroxyamino-oximes 3 as expected according to von Auwers' procedure1): only one molecule of hydroxylamine is consumed leading to trans-configurated 2-benzoyl-3-phenyl-1H-aziridines 4. Aus den hochsubstituierten Chalkonen 1 entstehen nicht die nach von Auwers1) zu erwartenden Dioxime 2 ...

Highly substituted chalcones 1 do not react with two molecules of hydroxylamine
affording dioximes 2 or hydroxyamino-oximes 3 as expected
according to von Auwers' procedure1): only one molecule of hydroxylamine
is consumed leading to trans-configurated 2-benzoyl-3-phenyl-1H-aziridines 4.

Aus den hochsubstituierten Chalkonen 1 entstehen nicht die nach von
Auwers1) zu erwartenden Dioxime 2 oder Hydroxyamino-oxime 3 unter
Verbrauch von zwei Mol Hydroxylamin. Stattdessen wird nur ein Mol
Hydroxylamin verbraucht, und es entstehen trans-konfigurierte 2-Benzoyl-
3-phenyl-1H-aziridine 4.


Involved Institutions


Details

Item typeArticle
Journal or Publication TitleArchiv der Pharmazie
Publisher:John Wiley & Sons
Volume:327
Page Range:pp. 207-210
Date1994
InstitutionsChemistry and Pharmacy > Institute of Pharmacy > Alumni or Retired Professors > Prof. Wiegrebe
Dewey Decimal Classification500 Science > 540 Chemistry & allied sciences
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgUnknown
URN of the UB Regensburgurn:nbn:de:bvb:355-epub-157933
Item ID15793

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