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Intramolecular 1,3-Dipolar Cycloaddition of Azomethine Ylides Leading to Pyrido[2,3-b]quinolines

✍ Scribed by Tóth, Judit; Somfai, Barbara; Blaskó, Gábor; Dancsó, András; Töke, László; Nyerges, Miklós

Book ID
111933257
Publisher
Taylor and Francis Group
Year
2009
Tongue
English
Weight
318 KB
Volume
39
Category
Article
ISSN
0039-7911

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1,3-Dipolar cycloaddition of stabilized
1,3-Dipolar cycloaddition of stabilized azomethine ylides to alkenyl quinolines: An efficient route to polyfunctionalized 3-pyrrolidinylquinoline derivatives
✍ Abdelmalek Bouraiou; Abdelmadjid Debache; Salah Rhouati; Ali Belfaitah; Bertrand 📂 Article 📅 2008 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 281 KB

## Abstract magnified image Some new polysubstituted 3‐pyrrolidinylquinolinyl derivatives were prepared by 1,3 dipolar cycloadditions of an azomethine ylide, generated __in situ__ from benzylideneimine of methylglycinate and triethylamine in the presence of LiBr, to quinolyl α,β‐unsaturated esters