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

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A practically simple three-component chiral derivatization protocol for determining the enantiopurity of chiral hydroxylamines by 1H NMR spectroscopic analysis is described, involving their treatment with 2-formylphenylboronic acid and enantiopure BINOL to afford a mixture of diastereomeric nitrono-boronate esters whose ratio is an accurate reflection of the enantiopurity of the parent hydroxylamine.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Formula: C20H14O2, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 18531-99-2

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