Room‐Temperature Cascade Electrophilic Addition/Cyclization/Oxidation Reactions: Divergent Selective Synthesis of Brominated 2H‐Chromenes, 2H‐Chromen‐2‐ols and 2H‐Chromen‐2‐ones

Abstract The room temperature metal‐free cascade electrophilic addition/cyclization/oxidation reactions of (3‐phenoxyprop‐1‐yn‐1‐yl)benzenes to divergently synthesize various brominated benzopyran derivatives (3‐bromo‐2 H ‐chromenes, 3‐bromo‐2 H ‐chromen‐2‐ols and 3‐bromo coumarins) by tuning the amount of Br 2 and H 2 O have been developed. The method exhibited high selectivity, mild reaction conditions, broad substrate scope, high efficiency, and the applicability for derivatization of the brominated products. The importance of the strategies provides a great advantage for selective synthesis of brominated benzopyran derivatives.