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Synthesis of functionalized thiopyrano [2,3-b]quinolines via a cascade reactions catalyzed by magnetic arginine/alginate biocomposite
Published:
14 November 2020
by MDPI
in The 24th International Electronic Conference on Synthetic Organic Chemistry
session General Organic Synthesis
Abstract:
An effective synthesis of functionalized thiopyrano[2,3-b]quinolines has been described via cascade reactions using superparamagnetic iron oxide nanoparticles (SPIONs) coated with L-arginine (Arg) grafted alginate (Alg) called Fe3O4@Alg@CPTMS@Arg. The reaction was performed between commercially available CH acids compounds such as dimedone or malononitrile, and 2-mercapto-quinoline-3-carbaldehydes under green conditions. This efficient method provides a new route for the formation of functionalized three or four fused rings.
Keywords: L-arginine, alginate, superparamagnetic nanocomposite, 2-mercapto-quinoline-3-carbaldehydes, thiochromene derivatives