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Mol Divers ; 21(1): 29-36, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27599493

ABSTRACT

The reactions of several 2-chloroquinoline-3-carboxylate esters with propargyl alcohol and a secondary amine in the presence of palladium catalyst leads to the formation of new alkyl 1-amino substituted pyrrolo[1,2-a]quinoline-4-carboxylate derivatives. This one-pot process, carried out in the absence of any copper salt, provides an efficient method for the synthesis of functionalized pyrrolo[1,2-a]quinolines in good-to-high yields.


Subject(s)
Carboxylic Acids/chemistry , Quinolines/chemistry , Quinolines/chemical synthesis , Alkynes/chemistry , Catalysis , Chemistry Techniques, Synthetic , Esters
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