Issue 22, 2009

Ni and Pd mediate asymmetric organoboron synthesis with ester functionality at the β-position

Abstract

Catalytic systems based on Ni and Pd complexes modified with chiral P-P ligands can be used in a convenient strategy for enantioselectively adding a boron unit to the β-position of α,β-unsaturated esters.

Graphical abstract: Ni and Pd mediate asymmetric organoboron synthesis with ester functionality at the β-position

Supplementary files

Article information

Article type
Paper
Submitted
11 May 2009
Accepted
27 Jul 2009
First published
03 Sep 2009

Org. Biomol. Chem., 2009,7, 4674-4676

Ni and Pd mediate asymmetric organoboron synthesis with ester functionality at the β-position

V. Lillo, M. J. Geier, S. A. Westcott and E. Fernández, Org. Biomol. Chem., 2009, 7, 4674 DOI: 10.1039/B909341A

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