4.6 Article

A Pd-catalyzed, boron ester-mediated, reductive cross-coupling of two aryl halides to synthesize tricyclic biaryls

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 15, Issue 27, Pages 5790-5796

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ob01237c

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Funding

  1. University Cancer Research Fund

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Tricyclic biaryls are important scaffold structures in many natural products and lead compounds in drug discovery. The formation of a biaryl unit is often the key step for the synthesis of tricyclic biaryls. Despite significant progress toward the synthesis of biaryl compounds in recent years, the direct cross-coupling of two different aryl halides is still challenging and robust methods are lacking. Herein we report a direct cross-coupling of two different aryl halides in the presence of a palladium catalyst and boron ester, which provides a new and useful complementary method to synthesize tricyclic biaryls.

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