Synthetic Route of 18531-99-2, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.18531-99-2, Name is (S)-[1,1′-Binaphthalene]-2,2′-diol, molecular formula is C20H14O2. In a Article£¬once mentioned of 18531-99-2
Asymmetric Synthesis of Axially Chiral 1,1′-Biphenyl-2-carboxylates via Nucleophilic Aromatic Substitution on 2-Menthoxybenzoates by Aryl Grignard Reagents
A practical method is presented for an asymmetric synthesis of axially chiral 1,1′-biphenyl-2-carboxylates via the ester-assisted nucleophilic aromatic substitution reaction.Thus, upon treatment of 2-tert-butylphenyl 2-<(-)-menthoxy>benzoates with an aryl Grignard reagent, chirality of the leaving (-)-menthoxy group is transferred to the newly formed biphenyl linkage with up to 94percent optical yield.
The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 18531-99-2 is helpful to your research. Synthetic Route of 18531-99-2
Reference£º
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI