Abstract
AbstractWe delineate a simple and straightforward tin(II) triflate catalyzed facile protocol for the synthesis of 3‐methyleneisoindolin‐1‐ones that applied to broad range of substrates, which simultaneously offers the functional group tolerance of the reaction and the stability of these scaffolds to the reaction conditions. In addition, in situ reduction of the exocyclic double bond in 3‐methyleneisoindolin‐1‐ones using PMHS is also reported.
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