Brief introduction of (S)-[1,1′-Binaphthalene]-2,2′-diol

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 18531-99-2

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

Homochiral 2,2?-bis(oxazolin-2-yl)- 1,1?-binaphthyl (boxax) ligands were anchored on various polymer supports including PS-PEG, PS, PEGA, and MeO-PEG via selective monofunctionalization at the 6-position of the binaphthyl backbone. Palladium(II) complexes of the supported boxax ligands catalyzed Wacker-type cyclization of 2-(2,3-dimethyl-2-butenyl)phenol to give 2-methyl-2-isopropenyl-2,3-dihydrobenzofuran with up to 96% ee.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 18531-99-2

Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI