Catalyst‐free 1,6‐Conjugate Addition of S‐Nucleophiles to para‐Quinone Methides.

An efficient access to a large array of diarylmethane thioether derivatives is developed through catalyst‐free 1,6‐conjugate addition of 1,4‐dithiane‐2,5‐diols with para‐quinone methides in high to excellent yields. Moreover, this reaction system is also suitable for other sulfur‐based nucleophiles, and the resulting products can be readily converted into other valuable diarylmethane derivatives. [ABSTRACT FROM AUTHOR]