One-Pot Synthesis of Benzothiazole-Tethered Chromanones/Coumarins via Claisen Rearrangement Using the Solid State Melt Reaction

A novel protocol has been successfully established for the efficient synthesis of benzothiazole-tethered chromanone/coumarin scaffolds via Claisen rearrangement using a solid state melt reaction in a one-pot manner. Benzothiazole formation and Claisen rearrangement involve the cleavage of S–S and C–...

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Veröffentlicht in:Journal of organic chemistry 2016-04, Vol.81 (8), p.3391-3399
Hauptverfasser: Bakthadoss, Manickam, Selvakumar, Raman
Format: Artikel
Sprache:eng
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Zusammenfassung:A novel protocol has been successfully established for the efficient synthesis of benzothiazole-tethered chromanone/coumarin scaffolds via Claisen rearrangement using a solid state melt reaction in a one-pot manner. Benzothiazole formation and Claisen rearrangement involve the cleavage of S–S and C–O bonds and formation of C–S, CN, and C–C bonds in a single operation without using a catalyst or solvent.
ISSN:0022-3263
1520-6904
DOI:10.1021/acs.joc.5b02920