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Heterocyclic enaminones: Photochemical synthesis of 6,7,8,9-tetrahydro-5H-pyrido[2,3-b]indol-9-ones

✍ 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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✦ 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.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Compared Reactivity
✍ Y. BLACHE; M.-E. SINIBALDI-TROIN; A. VOLDOIRE; O. CHAVIGNON; J.-C. GRAMAIN; J.-C πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 34 KB πŸ‘ 2 views

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