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1,3‐Dipolar cycloaddition of stabilized azomethine ylides to alkenyl quinolines: An efficient route to polyfunctionalized 3‐pyrrolidinylquinoline derivatives
Author(s) -
Bouraiou Abdelmalek,
Debache Abdelmadjid,
Rhouati Salah,
Belfaitah Ali,
Carboni Bertrand
Publication year - 2008
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570450206
Subject(s) - azomethine ylide , triethylamine , 1,3 dipolar cycloaddition , cycloaddition , chemistry , combinatorial chemistry , organic chemistry , catalysis , medicinal chemistry
ome 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