Germacranolides from Schkuhria anthemoidea

The isolation of eucannabinolide and three new sesquiterpene lactones from Schkuhria anthemoidea is reported. The structures and stereochemistries of the new compounds were established by chemical and spectroscopic means. The structure of santhemoidin B was confirmed by X-ray crystallography.     

Three furanoheliangolides from Calea villosa

Calea villosa afforded three new sesquiterpene lactones, two furanoheliangolides and an epoxy- germacranolide, as well as several known compounds. The structures were elucidated by spectroscopic methods.     

New germacranolides from Isocarpha species

The investigation of two Isocarpha species has yielded eight new germacranolides most of them belonging to the heliangolides. In addition to known p-hydroxyacetophenone-derivatives, a new dihydroeuparine derivative was isolated. The chemotaxonomical aspects are discussed.     

Sesquiterpene lactones from Eremanthus species

The investigation of three Eremanthus species afforded, in addition to known compounds, several new sesquiterpenelactones, a cumambrin B isobutyrate, four lactones related to the eremantholides, two to zexbrevin and one to goyazensolide. Furthermore, a new coniferyl alcohol derivative was isolated. The overall picture of the genus is very uniform. The occurrence of eremanthine and germacranolides with a furanone ring seems to be especially typical.     

Guaianolides,heliangolides, diterpenes and cycloartenol derivatives from Balsamorhiza sagittata

Investigation of the aerial parts of Balsamorhiza sagittata afforded 12 new sesquiterpene lactones, five guaianolides, three heliangolides, three germacranolides and two geranylnerol derivatives. From the roots eight cycloartane derivatives, a hydroxylanosterone and hexacos-1-ene were isolated. Structures were elucidated mainly by spectroscopic methods, especially high field NMR. The chemotaxonomic situation is discussed briefly.     

Guaianolides and heliangolides from Hymenopappus newberryi

The aerial parts of Hymenopappus newberryi afforded two heliangolides, two thymol derivatives, as well as two new guaianolides and a trans, trans-germacranolide closely related to hiyodorilactone A. Furthermore, the ent-kaurene derivative abbeokutone was present. These results are of chemotaxonomic interest.     

Sesquiterpene lactones from Helianthus niveus subsp. niveus

Six germacranolides, tirotundin, tagitinin A. orizabin, 8β,14-dihydroxycostunolide and its 14-isobutyrate, and 4β,5-dihydrotagitinin C, were isolated from aboveground parts of Helianthus niveus subsp. niveus. The last two compounds are new.     

New germacrolide- and heliangolide-type sesquiterpene lactones from Melampodium linearilobum

Chemical analysis of Melampodium linearilobum yielded, besides coumarin, seven germacrolide-type sesquiterpene lactones, linearilobin A to G and two heliangolides, linearilobin H and I. All new sesquiterpene lactones are oxygenated at C-14 and C-15 and differ by the number and types of ester moieties at C-8, C-14 and C-15. M. linearilobum represents the first species within the genus known to produce germacrolides and heliangolides instead of the more common melampolides.     

Furanoheliangolides from Viguiera greggii

Three furanoheliangolide sesquiterpene lactones were isolated from Viguiera greggii, including a novel compound, 1,2-dehydrozexbrevin B, and the previously characterized zexbrevin and zexbrevin B. Structures were determined by spectral methods, chiefly ¹H and ¹³C NMR. Based on present knowledge, there appear to be no major differences between the terpenoid chemistry of Viguiera and that of Helianthus, a genus believed to be very closely related to Viguiera on morphological grounds.     

Three biologically active heliangolides from Helianthus annuus

Growth inhibiting substances in Helianthus annuus have been investigated. From the ethanolic extract a new germacranolide with an α-methylene-γ-lactone moiety, the heliangolide niveusin B and its ethoxy derivative were isolated and their structures elucidated by spectroscopic methods. The biological activity of each was determined by inhibition in Avena coleoptile tests and antimicrobial tests.