Transformation Products of Salutarine and Their ^<13>C-Nuclear Magnetic Resonance Spectra

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概要

• 論文の詳細を見る

• Salutarine, the principal alkaloid of Croton salutaris CASAR has been treated with phenyllithium and methyllithium to yield the corresponding salutarinols. treatment of 7-phenylsalutarinol (not isolated) with acid produced the racemic form of 7-phenylthebaine. The mixture of epimeric 7-methylsalutarinols yielded mainly the dehydration product, the 7-methylene derivative of salutarine. A comparison of the ^<13>C-nuclear magnetic resonance spectra of these and other derivatives of salutarine permitted a complete assignment of the chemical shifts.

• 公益社団法人日本薬学会の論文
• 1982-06-25

著者

• BARNES RODERICK

  Nucleus of Research on Natural Products Federal University of Rio de Janeiro

• SOEIRO ORLANDO

  Nucleus of Research on Natural Products, Federal University of Rio de Janeiro

• SILVA ANTONIOJ.R.da

  Nucleus of Research on Natural Products, Federal University of Rio de Janeiro

• Soeiro Orlando

  Nucleus Of Research On Natural Products Federal University Of Rio De Janeiro

• Silva Antonioj.r.da

  Nucleus Of Research On Natural Products Federal University Of Rio De Janeiro

関連論文

• A New Triterpene from Vellozia compacta
• Transformation Products of Salutarine and Their ^C-Nuclear Magnetic Resonance Spectra

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