EventsThe 24th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session A. General Organic Synthesis of the event The 24th International Electronic Conference on Synthetic Organic Chemistry
Published date
14 Nov, 2020
Citation
Shahrzad Javanshir, Sara Amirnejat, Ali Nosrati, Synthesis of functionalized thiopyrano [2,3-b]quinolines via a cascade reactions catalyzed by magnetic arginine/alginate biocomposite, in Proceedings of The 24th International Electronic Conference on Synthetic Organic Chemistry, 15 November–15 December 2020, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-24-08413
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Synthesis of functionalized thiopyrano [2,3-b]quinolines via a cascade reactions catalyzed by magnetic arginine/alginate biocomposite

1. Heterocyclic Chemistry Research Laboratory, Department of Chemistry, Iran University of Science and Technology, Tehran 16846-13114, Iran
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
Manuscript
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