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Austroeupatorium inulaefolium

Vitexilactone, obtained from Vi tex cannabifolia (Verbenaceae), has been shown to have the structure (16). It has been correlated with rotundifuran. An interesting iron(ii)-catalysed decomposition of unsaturated cyclic peroxides derived from butadienes leads to 3-alkylfurans. This procedure has been used to convert the peroxide (17) from ds-biformene into the furan (18). Some diterpenoid furans are amongst the constituents of Austroeupatorium inulaefolium (Compositae). These include the diketone austrofolin (19), the corresponding 12-alcohol, and the 15-alcohol (20). A triol, austroinulin (21), was also identified. [Pg.126]

Bohlmann, F., G. Schmeda-Hirschmann, and J. Jakupovic Nor-ewMabdan derivate Austroeupatorium inulaefolium. Planta Med. 1984, 199 (1984). [Pg.558]

See other pages where Austroeupatorium inulaefolium is mentioned: [Pg.158]    [Pg.111]    [Pg.169]    [Pg.169]    [Pg.169]    [Pg.169]    [Pg.170]    [Pg.178]    [Pg.179]    [Pg.185]    [Pg.187]    [Pg.189]    [Pg.194]    [Pg.196]    [Pg.202]    [Pg.202]    [Pg.216]    [Pg.216]    [Pg.216]    [Pg.571]    [Pg.158]    [Pg.111]    [Pg.169]    [Pg.169]    [Pg.169]    [Pg.169]    [Pg.170]    [Pg.178]    [Pg.179]    [Pg.185]    [Pg.187]    [Pg.189]    [Pg.194]    [Pg.196]    [Pg.202]    [Pg.202]    [Pg.216]    [Pg.216]    [Pg.216]    [Pg.571]   


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