Expedient copper-catalyzed borylation reactions using amino acids as ligands

Amino acids were found to be as good ligands for copper-catalyzed borylation reactions of primary and secondary alkyl halides, and the B2pin2 acted as bi-boron source for borylation. The high reaction efficiency and mild conditions make the new catalyst system a useful alternative to the recently developed methods for the preparation of alkylboronic esters.

A highly general, experimentally simple, and inexpensive catalyst system was developed for copper-catalyzed borylation reactions of primary and secondary alkyl halides with amino acid as ligand.Figure optionsDownload as PowerPoint slide