Publication | Closed Access
One-Pot Synthesis of Benzothiazole-Tethered Chromanones/Coumarins via Claisen Rearrangement Using the Solid State Melt Reaction
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Citations
32
References
2016
Year
Chemical EngineeringCross-coupling ReactionEngineeringDiversity Oriented SynthesisNovel ProtocolClaisen RearrangementNatural SciencesDiversity-oriented SynthesisOne-pot SynthesisOrganic ChemistryBenzothiazole-tethered Chromanones/coumarinsCatalysisChemistryHeterocycle ChemistrySynthesis MethodSynthetic ChemistrySolid State
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.
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