Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 2000; 2000(4): 541-544
DOI: 10.1055/s-2000-6371
DOI: 10.1055/s-2000-6371
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
An Elegant Approach Towards the Regioselective Synthesis of Deazalumazines Through Nucleophile Induced Ring Transformation Reactions of 6-Aryl-3-cyano-4-methylthio-2H-pyran-2-ones
Further Information
Publication History
Publication Date:
31 December 2000 (online)
![](https://www.thieme-connect.de/media/synthesis/200004/lookinside/thumbnails/10.1055-s-2000-6371-1.jpg)
Deazalumazines also known as pyrido[2,3-d]pyrimidines (3) have been regioselectively synthesized through nucleophile induced ring transformation reactions of 6-aryl-3-cyano-4-methylthio-2H-pyran-2-ones (1) with 6-amino-1,3-dimethyluracil (2).
6-aryl-3-cyano-4-methylthio-2H-pyran-2-ones - 6-amino-1,3-dimethyluracil - ring transformation reactions - regioselective synthesis - condensation - heterocycles