Iridium-Catalyzed Regioselective Borylation of Substituted Biaryls

Author:

Chotana Ghayoor1,Asghar Soneela1,Shahzadi Tayyaba1,Alazmi Meshari2,Gao Xin2,Emwas Abdul-Hamid3,Saleem Rahman1,Batool Farhat1

Affiliation:

1. Department of Chemistry & Chemical Engineering, Syed Babar Ali School of Science & Engineering, Lahore University of Management Sciences

2. King Abdullah University of Science and Technology (KAUST), Computational Bioscience Research Center (CBRC), Computer, Electrical and Mathematical Sciences and Engineering (CEMSE) Division

3. King Abdullah University of Science and Technology (KAUST)

Abstract

Biarylboronic esters are generally prepared by directed ortho­-metalation or by Miyaura borylation and hence rely on the presence of a directing group or pre-functionalization. In this paper, the preparation of biarylboronic esters by direct C–H borylation of biaryl substrates is reported. Sterically governed regioselectivities were observed in the borylation of appropriately substituted biaryls by using [Ir(OMe)(COD)]2 precatalyst and di-tert-butylbipyridyl ligand. The resulting biarylboronic esters were isolated in 38–98% yields. The synthesized biarylboronic esters were further successfully employed in C–O, C–Br, and C–C coupling reactions.

Funder

Higher Education Commission (HEC) of Pakistan

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

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