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Asymmetric Catalysis for Oxidative Coupling of 2-Naphthol to BINOL

Asymmetric Catalysis for Oxidative Coupling of 2-Naphthol to BINOL [Pg.49]

Catalyst ligand Temperature Time Solvent Conversion Selectivity Ee% [Pg.50]

The chiral self-dimerization oftheV complex precursors at the Si02 surface produced a unique reaction space for the selective oxidation. [Pg.51]

Notably, even if the V monomer precursors (1) are racemic at the V center in solution, only a particular arrangement of two V monomers among possible structural arrangements is allowed as a stable structure at the Si02 surface, creating a new chiral V center (2) to provide a chiral reaction space for the enantioselective catalysis. Chiral self-assembly is a common phenomenon that is applied to other catalytic materials on surfaces. [Pg.51]

Low-Temperature Preferential Oxidation of CO in Excess H2 on Cu-Clusters Dispersed on Ce02 [Pg.51]




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1- Naphthol oxidation

2- Naphthol oxidative coupling

Asymmetric Oxidative Coupling of 2-Naphthol to BINOL

Asymmetric catalysis

Asymmetric coupling of 2-naphthol

Asymmetric oxidation

Asymmetric oxidative coupling

BINOL

BINOL catalysis

For coupling

Naphthol-coupling

Of 1-naphthol

Oxidation catalysis

Oxidation, asymmetric catalysis

Oxidative Coupling of 2-Naphthols

Oxides catalysis

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