Intramolecular diels-alder reactions of indoles
β Scribed by George A. Kraus; Jeff Raggon; P.J. Thomas; Dan Bougie
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 209 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The first examples of intramolecular Diels-Alder reactions on indoles indicate that this reaction may be employed for the direct preparation of highly functionalized dihydroindoles. The hybridization of the atoms in the tether plays a crucial role.
π SIMILAR VOLUMES
## Intramolecular Diels-Alder Reactions of 3-(Tetrahydropyridinyl)indoles: Stereoselective Synthesis of Novel Pentacyclic Ring Systems. -A strategy to synthesize new pentacyclic indole alkaloids is shown. Key step is an intramolecular Diels-Alder reaction and following acid-catalyzed [1,3]-hydro