Synthesis of pyrimidinones by action of benzamidine on a benzocycloheptenic β-keto ester
✍ Scribed by Nadine Muller; Robert Granet; Lucette Lepage; Pierre Krausz; Jean-Paul Laval
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2001
- Tongue
- English
- Weight
- 104 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The synthesis of a polycyclic heterocyclic ring system compound, ethyl 7‐hydroxy‐4‐oxo‐2‐phenyl‐4,5‐dihydro‐3__H__‐benzo[6,7]cyclohepta[1,2‐d]pyrimidine‐6‐carboxylate was carried out by condensation of benzamidine on diethyl 5,9‐dihydroxy‐7__H__‐benzo[a]cycloheptene‐6,8‐dicarboxylate, after opening and then closure of the seven membered ring.
📜 SIMILAR VOLUMES
## Abstract (±)‐Acoragermacrone, a natural occurring germacrane‐type sesquiterpenoid, was synthesized from geranyl acetate via eight steps by employing titanium‐induced intramolecular keto α,β‐unsaturated ester coupling as key step.