Abstract

Hexaarylbenzene scaffolds , containing six different aromatic rings around the central benzene core, are a synthetic challenge. In their Research Article on page 22307, Svetlana B. Tsogoeva et al. report a process that allows the simple and straightforward generation of such hexaarylbenzenes (HABs). In an efficient, two-component four-step domino reaction, a functionalized triarylbenzene is formed and used as a key intermediate to furnish asymmetrically substituted HABs in high overall yield and without involvement of statistical steps.

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