1. Natural amygdalin has the R configuration at the chiral phenyl center. 2. These substitute groups are trifluoromethylated phenyl ethanol and amino acetal arrangement. 3. Both the phenyl and the naphthanol group are aromatic ring systems. 4. The crystal structure of phenyl -substituted boroxine is more complex. 5. Further reaction with lead ( II ) nitrate gives phenyl isothiocyanate: 6. The name'phenanthrene'is a composite of phenyl and anthracene. 7. It can be prepared by the heating of phenyl salicylate. 8. For example, phenyl azide and phenylacetylene give diphenyl triazole. 9. The terminal phenyl constituents contribute hydrophobic binding to increase potency. 10. The reaction works well for methyl, benzyl, and phenyl substituents.
Mobile