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Further Guaianolides from Amphoricarpos neumayeri ssp. murbeckii from Montenegro
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2006
Year
BiologyAmphoricarpos Neumayeri SspNew CompoundsNatural Product SynthesisNatural SciencesDiversity-oriented SynthesisSecondary MetaboliteOrganic ChemistryZoological Taxonomyδ 11ChemistryPhytochemistryPharmacologyBasic Skeleton
The aerial parts of Amphoricarpos neumayeri ssp. murbeckii afforded eleven guaianolides with the same relative (1αH,4β H,5αH,7αH) configuration of the basic skeleton. All of them contained a CH 2 OX (X = H, acetyl or isovaleroyl) group in 4α-position, typical for amphoricarpolides. Four compounds (1 - 4) were isolated before from the same species, originating from different localities. Guaianolides 5 - 11 are new compounds. Compounds 7 and 8 were epoxidized at the 10α(14)-position. Instead of the Δ 11(13) -double bond, observed in all previously isolated guaianolides from the same species, the four lactones contained 11α,13-diol (8 - 10) or 11α-OH,13-chloro (11) moieties respectively.