Highly Enantioselective Aerobic Oxidation of α-Hydroxyphosphonates Catalyzed by Chiral Vanadyl(V) Methoxides Bearing N-Salicylidene-α-aminocarboxylates
Journal of the American Chemical Society2006Vol. 128(19), pp. 6308–6309
Citations Over TimeTop 10% of 2006 papers
Abstract
An unprecedented vanadyl(V) methoxide complex 4 derived from 3,5-dibromo-N-salicylidene-l-tert-leucinate enables highly enantioselective aerobic oxidations of alpha-hydroxyphosphonates at ambient temperature with selectivity factors ranging from 3 to >99.
Related Papers
- → Recent developments in enantioselective iron-catalyzed transformations(2019)58 cited
- → Alternative Synthetic Strategies for Enantioselective Construction of Halogenated Chiral Carbon Centers(2010)37 cited
- → Methods of Asymmetric Synthesis—Enantioselective Catalytic Hydrogenation(1971)142 cited
- → The First Catalytic Enantioselective Synthesis of (R)-(+) Lasiodiplodin(1993)18 cited
- → Chiral B(III) Lewis Acids(2000)19 cited