A new longipinene diester from Stevia monardifolia Kunth

Rodrigo E. Rojas-Pérez, Ernestina Cedillo-Portugal, Pedro Joseph-Nathan, Eleuterio Burgueño-Tapia

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Nonpolar and medium polarity fractions from whole plant methanolic extracts of Stevia monardifolia afforded the new 7β-angeloyloxy-8 α-isovaleroyloxylongipin-2-en-1-one 1 along with known 7β,8α-diangeloyloxylongipin-2-en-1-one 2 and 7β,8α- diangeloyloxylongipinan-1-one 3. Alkaline hydrolysis of a mixture of 1 and 2 gave 7β,8α-dihydroxylongipin-2-en-1-one 4 which was subjected to a single crystal X-ray diffraction study. The new compound 1, which is the third 7β,8α-dihydroxylongipin-2-en-1-one diester natural product isolated from a Stevia especies, was fully characterized by oneand two-dimensional NMR spectroscopy and its absolute configuration was confirmed as the 4R,5S,7S,8S,10R,11R enantiomer by vibrational circular dichroism (VCD) measurements in comparison to calculation at the B3LYP/DGDZVP level of theory.

Original languageEnglish
Pages (from-to)757-762
Number of pages6
JournalNatural Product Communications
Volume4
Issue number6
DOIs
StatePublished - 2009

Keywords

  • Absolute configuration
  • Longipinene
  • NMR
  • Stevia monardifolia
  • Vibrational circular dichroism

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