Amadori rearrangement of N-glucosides of 6-substituted 3-amino-2-aryl-4(3H)-quinazolinones

Saleh, Mohamed A., Abdo, Mohamed A., Abdel-Megeed, Mohamed F. and El-Hiti, Gamal A. 1996. Amadori rearrangement of N-glucosides of 6-substituted 3-amino-2-aryl-4(3H)-quinazolinones. Indian Journal of Chemistry Section B 35B (2) , pp. 147-150. 10.1002/chin.199617207

Full text not available from this repository.

Abstract

Amadori rearrangement of N-glucosides of 6-substituted 3-amino-2-aryl-4(3H)-quinazolinones has been carried out by the condensation of equimolecular amounts of D-glucose and oxalate of 6-substituted 3-amino-2-aryl-4(3H)-quinazolinones (la-f) in boiling methanol. These compounds can also be obtained by heating the N-glucosides of 6-substituted 3-amino-2-aryl-4(3H)-quinazolinones (2a-f) in absolute methanol in the presence of dry oxalic acid. The products obtained are characterized by IR, 1H NMR, 13C NMR and mass spectral data and elemental analyses.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Schools > Chemistry
Subjects:	Q Science > QD Chemistry
Publisher:	Publications & Information Directorate, Csir / NISCAIR
ISSN:	0376-4699
Last Modified:	19 Mar 2016 22:25
URI:	https://orca.cardiff.ac.uk/id/eprint/15617

Citation Data

Actions (repository staff only)

Edit Item