Two cardenolides from Calotropis procera

Atef G. Hanna, M. Hani A. Elgamal, Nagy A.M. Morsy, Helmut Duddeck, József Kovács, Gábor Tóth

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

Two cardiotonic glycosides were isolated from Calotropois procera: one of them (1) is a new natural product. Their structures were elucidated by extensive application of one- and two-dimensional 1H and 13C NMR spectroscopy.

Original languageEnglish
Pages (from-to)754-757
Number of pages4
JournalMagnetic Resonance in Chemistry
Volume37
Issue number10
Publication statusPublished - Oct 1 1999

Keywords

  • C NMR
  • Cardenolides
  • Conformation
  • H NMR
  • HMQC-TOCSY
  • NMR
  • ROESY
  • Stereochemistry
  • gs-COSY
  • gs-HMBC
  • gs-HMQC
  • gs-HSQC

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)

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  • Cite this

    Hanna, A. G., Elgamal, M. H. A., Morsy, N. A. M., Duddeck, H., Kovács, J., & Tóth, G. (1999). Two cardenolides from Calotropis procera. Magnetic Resonance in Chemistry, 37(10), 754-757.