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Proton Phototransfers in Doubly Hydrogen Bonded Dimers: The Photophysics of 6,7,8,9-Tetrahydro-5 H -pyrido[2,3- b ]indole Dimers

✍ Scribed by Catalán, Javier

Book ID
125945059
Publisher
American Chemical Society
Year
2010
Tongue
English
Weight
638 KB
Volume
114
Category
Article
ISSN
1089-5639

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Heterocyclic enaminones: Photochemical s
Heterocyclic enaminones: Photochemical synthesis of 6,7,8,9-tetrahydro-5H-pyrido[2,3-b]indol-9-ones
✍ Yves Blache; Marie-Eve Sinibaldi-Troin; Mohammed Hichour; Veronique Benezech; Ol 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 449 KB

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.

ChemInform Abstract: Compared Reactivity
ChemInform Abstract: Compared Reactivity of Heterocyclic Enaminones: Photochemical and Palladium Catalyzed Synthesis of 6,7,8,9-Tetrahydro-5H-pyrido[3,2-b]indol-9-ones.
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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