Anionic boron-based chiral bisoxazoline ligands, the borabox ligands, are readily prepared from amino alcohols and haloboranes. The highly modular nature of these ligands allows both for electronic and steric tuning of the structure. The high enantioselectivities obtained in various Cu-catalyzed asymmetric reactions and especially in the kinetic resolution of pyridyl alcohols where bisoxazoline ligands exhibit almost no selectivity, point to a considerable potential of borabox ligands in asymmetric catalysis. © Schweizerische Chemische Gesellschaft.
CITATION STYLE
Mazet, C., Köhler, V., Roseblade, S., Toussaint, A., & Pfaltz, A. (2006). Synthesis of boron-bridged anionic C2-symmetric bisoxazolines and their application in asymmetric catalysis. In Chimia (Vol. 60, pp. 195–198). Swiss Chemical Society. https://doi.org/10.2533/000942906777674958
Mendeley helps you to discover research relevant for your work.