Synthesis and theoretical calculations of novel 5-aryl substituted 2,4,7-trioxo and 4,7-dioxo-2-thioxopyrido[2,3-d]pyrimidines
✍ Scribed by René Rodríguez; Margarita Suárez; Estael Ochoa; Alhmed Morales; Leandro González; Nazario Martín; Margarita Quinteiro; Carlos Seoane; José L. Soto
- Book ID
- 112131423
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1996
- Tongue
- English
- Weight
- 305 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The tide compounds 4a‐c have been prepared in a one‐step procedure from 2,4‐diamino‐6‐hydroxy‐pyrimidine (1) and the corresponding arylidene substituted Meldrum's acids 2a‐e in very good yields. Semiempirical theoretical calculations (AMI) reveal two favoured conformations (A and B) for
Novel 2,3-substituted-2,4-dihydro-pyrazolo[4,3-d] pyrimidine-5,7-diones were successfully synthesized with moderate to good yields using a new synthetic approach. The structures of the regio-isomers in this series were determined by single crystal X-ray analysis and NMR spectra.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.