Metal-free site-selective functionalization with cyclic diaryl λ-chloranes: suppression of benzyne formation for ligand-coupling reactions.

While hypervalent halogens are versatile reagents enabling diverse reactions in organic synthesis, the utility of hypervalent chlorine compounds, particularly cyclic λ-chloranes, remains underdeveloped despite their unique electronic properties and innate enhanced reactivity. Herein, we illustrate the elusive ligand coupling reaction of cyclic λ-chloranes that suppresses the more facile competing reaction modality involving benzyne intermediates. The methodology can be performed in three-component as well as two-component fashions, offering direct access to a wide range of unsymmetrically substituted biaryl molecules in very high yields and excellent -regioselectivity.