Heterocyclic enaminones: Photochemical synthesis of 6,7,8,9-tetrahydro-5H-pyrido[2,3-b]indol-9-ones
β Scribed by Yves Blache; Marie-Eve Sinibaldi-Troin; Mohammed Hichour; Veronique Benezech; Olivier Chavignon; Jean-Claude Gramain; Jean-Claude Teulade; Jean-Pierre Chapat
- Book ID
- 104209109
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 449 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
The synthesis of 6,7,8,9-tetrahydro-5H-pyrido[2,3-b]indol-9-ones from arylenaminones is described. Two "routes" have been investigated: a radical process through a photochemical reaction, and a catalytic process through an arylpalladium complex.
π SIMILAR VOLUMES
Compared Reactivity of Heterocyclic Enaminones: Photochemical and Palladium Catalyzed Synthesis of 6,7,8,9-Tetrahydro-5Hpyrido [3,2-b]indol-9-ones. -Tetrahydropyrido[3,2-b]indolones can be prepared efficiently by irradiation of enaminones of type (I) and (IV) as well as their Pd-catalyzed cyclizatio