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Imino Diels-Alder reactions catalyzed by indium trichloride (InCl3). Facile synthesis of quinoline and phenanthridinone derivatives

✍ Scribed by Govindarajulu Babu; Paramasivan T. Perumal

Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
110 KB
Volume
38
Category
Article
ISSN
0040-4039

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ChemInform Abstract: Imino Dielsβ€”Alder R
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✍ G. BABU; P. T. PERUMAL πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 2 views

Imino Diels-Alder Reactions Catalyzed by Indium Trichloride (InCl 3 ). Facile Synthesis of Quinoline and Phenanthridinone Derivatives. -Catalytic InCl 3 effectively promotes the imino-Diels-Alder reaction between the Schiff bases (I) and cyclopentadiene (II) or the cyclohexenone (IV) resulting in a

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Indium trichloride (InCl3)catalyzed imino Diels-Alder reactions: An efficient synthesis of cyclopentaquinolines, azabicyclooctanones and azabicyclononanones
✍ Govindarajulu Babu; Paramasivan T. Perumal πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 661 KB

Anhydrous indium trichloridc (InCl3) is found to catalyze the imino Diels-Alder reactions of Schiff's bases with cyclopentadiene, cyclohexen-2-one and cyclohepten-2-one which resulted in facile synthesis of cyclopentaquinolines, azabicyclooctanones and previously unreported series of azabicyclononan