1,3-Dibromo-5, 5-dimethylhydantoin (DBDMH)-promoted cross-coupling of enaminones with phenols under metal-free conditions.

[Display omitted] Despite significant progress in the area of enaminone vinyl C H functionalization, approaches for the direct synthesis of phenoxyl enaminone molecules remain a challenge. Here we describe a highly efficient 1,3‑Dibromo 5,5-dimethylhydantoin (DBDMH)-promoted cross-coupling reaction between enaminones and phenols. This method provides straightforward access to a wide range of polyfunctionalized aminophenoxyalkenes under mild conditions. The main advantageous features of this method includes a wide substrate scope and good functional group tolerance, operational simplicity, and easily available starting materials. [ABSTRACT FROM AUTHOR]