Abstract
The sustainable synthesis of indolylbenzothiazloes is reported utilising TPGS-750-M enabled nanomicellar catalysis in water. The reactions do not require additional catalysts and/or oxidants and proceed at room temperature. Subsequently, the indole rings were functionalized to construct novel tris-heterocyclic scaffolds via benzothiazole directed Mn(II)-catalyzed C2–H amination utilizing pyridones as the amine partner.
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