Enantioselective Iron/Bisquinolyldiamine Ligand-Catalyzed Oxidative Coupling Reaction of 2-Naphthols
Lin‐Yang Wu, Muhammad Usman, Wen‐Bo Liu
Abstract
An iron-catalyzed asymmetric oxidative homo-coupling of 2-naphthols for the synthesis of 1,1′-Bi-2-naphthol (BINOL) derivatives is reported. The coupling reaction provides enantioenriched BINOLs in good yields (up to 99%) and moderate enantioselectivities (up to 81:19 er) using an iron-complex generated in situ from Fe(ClO4)2 and a bisquinolyldiamine ligand [(1R,2R)-N1,N2-di(quinolin-8-yl)cyclohexane-1,2-diamine, L1]. A number of ligands (L2–L8) and the analogs of L1, with various substituents and chiral backbones, were synthesized and examined in the oxidative coupling reactions.
Topics & Concepts
Enantioselective synthesisCatalysisLigand (biochemistry)ChemistryOxidative phosphorylationOxidative coupling of methaneCyclohexaneCombinatorial chemistryDiamineMedicinal chemistryStereochemistryOrganic chemistryReceptorBiochemistryAxial and Atropisomeric Chirality SynthesisChemical synthesis and alkaloidsAlkaloids: synthesis and pharmacology