Identification of structure and study of configuration of reaction products of endo-dicyclopentadiene with phenols by the1H and13C NMR method
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It was established by the13NMR spectroscopy method that Wagner-Meerwein rearrangement occurs when endo-dicyclopentadiene is reacted with phenol and the cresols, which leads to an exo-orientation of the cyclopentene ring.
The exo-orientation of the aromatic substituent was proved by an analysis of the1H NMR spectrum.
KeywordsSpectroscopy Phenol Spectroscopy Method Cresol Cyclopentene
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