Synthesis of Dialkyl 2-(Alkylamino)-4,9-dihydro-9-oxocyclohepta[b]pyran-3,4-dicarboxylates
✍ Scribed by Javad Azizian; Ali Ramazani; Mohammad Haji
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- German
- Weight
- 149 KB
- Volume
- 94
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Dialkyl 2‐(alkylamino)‐4,9‐dihydro‐9‐oxocyclohepta[b]pyran‐3,4‐dicarboxylates are prepared in a one‐pot three‐component reaction of alkyl isocyanide, dialkyl acetylenedicarboxylate, and α‐tropolone (=2‐hydroxycyclohepta‐2,4,6‐trienone). The reaction proceeds smoothly at room temperature and under neutral conditions to afford tropolone derivatives in high yield.
📜 SIMILAR VOLUMES
## Abstract For Abstract see ChemInform Abstract in Full Text.
Synthesis of 3,4-Dihydro-4-hydroxy-9-methoxy-2H-naphtho(2,3-b) thiopyranoquinone. -In order to obtain products with useful biological activity the title derivative (V) is synthesized starting from the known ketone (I). The structure of (V) is determined by X-ray analysis. -(TAPIA, R.