Ebenaceae extractives. Part 7. Use of hydroxy-proton shifts of juglone derivatives in structure elucidation

@inproceedings{Lillie1977EbenaceaeEP,
  title={Ebenaceae extractives. Part 7. Use of hydroxy-proton shifts of juglone derivatives in structure elucidation},
  author={Terence J. Lillie and Oliver C. Musgrave},
  year={1977}
}
  • Terence J. Lillie, Oliver C. Musgrave
  • Published 1977
  • Chemistry
  • Substitution at one or more positions of Juglone by bromo-, chloro-, hydroxy-, and methyl groups causes changes in the chemical shift of the hydroxy-proton which are additive and depend only on the nature and positions of the substituents. The hydroxy-proton signals of natural Juglone derivatives show similar regularities and enable the structures of neodiospyrin (11), galpinone (8), and bisisodiospyrin (7) to be defined. 

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