Abstract

AbstractHerein, we present our findings on the synthesis of 3,4‐oxepino‐fused indoles by a two‐step reaction sequence involving an initial allylic substitution followed by Rh(III)‐catalyzed intramolecular [3+2] annulation via C−H activation starting from Morita‐Baylis‐Hillman (MBH) acetates of acetylenic aldehydes. The strategy is amenable to broad range of MBH acetates providing a facile access to 3,4‐oxepino‐fused indoles in good yield.

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