Synthesis and molecular structure of novel 4-aryloctahydropyrido-[1,2-c]pyrimidine derivatives
✍ Scribed by Franciszek Herold; Jerzy Kleps; Beata Szczȩsna; Romana Anulewicz-Ostrowska
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2002
- Tongue
- English
- Weight
- 142 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
A series of new 4‐aryloctahydropyrido[1,2‐c]pyrimidine‐1,3‐diones 6a,b,d‐h and j were synthesized by intramolecular cyclization of α‐aryl‐α‐(1‐ethoxycarbonyl‐2‐piperidyl)‐acetamide derivatives 5a,b,d‐h and j. The structures of compounds were determined by ^1^H and ^13^C nmr spectroscopy. Nmr and X‐ray diffraction data indicate that the configuration at the C4, C4a stereocenters constitute RR and SS pair.
📜 SIMILAR VOLUMES
## Abstract A series of new 4‐aryl‐hexahydro‐1__H__,3__H__‐pyrido[1,2‐__c__]pyrirnidine‐1,3‐dione derivatives 4a‐k were prepared by catalytic hydrogenation of 4‐aryl‐1__H__,2__H__‐pyrido[1,2‐__c__]pyrirnidine‐1,3‐diones 3a‐k. The structures of compounds were determined by ^1^H and ^13^C nmr spectro
## Abstract A series of pyrazolo[4,3‐__e__]‐1,2,4‐triazolo‐[1,5‐__c__]pyrimidine derivatives, bearing phosphonylbenzyl chain in position 7, were conveniently synthesized in an attempt to obtain potent and selective antagonists for the A~2__A__~ adenosine receptor or potent pesticide lead compounds.