Abstract
Methods of preparing 1,1-bi-2-naphthol (BINOL) in optically active form, are reviewed. Preparation of this compound and its derivatives through both resolution and asymmetric synthesis, are discussed. Methods of determining the enantiomeric excess of samples of optically active BINOL, both through chromatographic and spectroscopic means, are also reviewed.
Keywords: BINOL, asymmetric synthesis, resolution, enantiomeric excess
Call for Papers in Thematic Issues
Exploring the Role of Chemical Graph Theory in Advancing Current Organic Synthesis
Organic synthesis is a fundamental discipline in chemistry, crucial for the creation of complex molecules with diverse applications in pharmaceuticals, materials science, and beyond. However, the process of designing efficient synthetic routes for target molecules remains challenging. Chemical graph theory, a branch of theoretical chemistry, offers powerful tools for understanding ...read more
Photoswitches for Molecular Recognition
This Special Issue would cover the hot topics on synthesis and chemical and photophysical characterization of new photoswitchable derivatives and their applications on molecular recognition of metabolites and biological active compounds, both in physiological medium and in living cells. Photoswitches are compounds that can change their conformation or properties in ...read more
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