Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1257330 | Chinese Chemical Letters | 2015 | 4 Pages |
Abstract
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.
Graphical abstractA 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 full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Meng-Yan Liu, Shi-Bin Hong, Wei Zhang, Wei Deng,