A BF3⋅Et2O promoted redox‐neutral cascade process including condensation/[1,7]‐hydride transfer/cyclization was disclosed for construction of the pharmaceutical significant benzothiadiazine 1,1‐dioxides, which featured novel substrate skeletons, broad substrate scope, [1,7]‐hydride transfer manner, metal‐free conditions and the facile intro‐duction of aryl, heteroaryl, allyl and propargyl groups
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