Browse:

The university is member of the Confederation of Open Access Repositories (COAR)

More information about Open Acces at open-acces.net

Formation of 1H-Aziridines from Chalcones and Hydroxylamine

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

Preview

PDF - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
686Kb

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 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.

Item Type:	Article
Institutions:	Chemistry and Pharmacy > Institute of Pharmacy > Retired Professors > Prof. Wiegrebe
Subjects:	500 Science > 540 Chemistry & allied sciences
Status:	Published
Refereed:	Yes, this version has been refereed
Created at the University of Regensburg:	Unknown
Owner:	Universitätsbibliothek Regensburg
Deposited On:	12 Jul 2010 11:40
Last Modified:	21 Jul 2011 00:32
Item ID:	15793

Export bibliographical data

Literature of the same author

in this repository

at BASE

at Google Scholar

at Scirus

Bookmark

Owner Only: item control page