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1,3-Dipolar cycloaddition of stabilized azomethine ylides to alkenyl quinolines: An efficient route to polyfunctionalized 3-pyrrolidinylquinoline derivatives

✍ Scribed by Abdelmalek Bouraiou; Abdelmadjid Debache; Salah Rhouati; Ali Belfaitah; Bertrand Carboni

Publisher: Journal of Heterocyclic Chemistry
Year: 2008
Tongue: English
Weight: 281 KB
Volume: 45
Category: Article
ISSN: 0022-152X
DOI: 10.1002/jhet.5570450206

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✦ Synopsis

Abstract

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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

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