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Easy access to polyhalogenated biaryls: regioselective (di)halogenation of hypervalent bromines and chlorines

Daniel Carter Martos, Maxime De Abreu, Pascal Hauk, Philipp Fackler, Joanna Wencel‐Delord

2024Chemical Science24 citationsDOIOpen Access PDF

Abstract

Polyhalogenated biaryls are unique motifs offering untapped potential as versatile building blocks for the expedient synthesis of complex biaryl compounds. Overcoming the limitations of conventional syntheses, we introduce a novel, metal-free, operationally simple and one-pot approach to regioselectively (di)halogenate biaryl compounds under mild conditions using cyclic biaryl hypervalent bromine and chlorine substrates as masked arynes. Through chemoselective post-functionalizations, these valuable products can expand the toolbox for synthesizing biaryl-containing scaffolds, addressing a critical gap in the field.

Topics & Concepts

Hypervalent moleculeRegioselectivityHalogenationChemistryCombinatorial chemistryOrganic chemistryIodineCatalysisCatalytic C–H Functionalization MethodsCatalytic Cross-Coupling ReactionsChemical synthesis and alkaloids