Oxidative degradations of the side chain of unsaturated Ent-labdanes. Part II
dc.creator | Catalán, L.E. | |
dc.creator | Marín, K.C. | |
dc.creator | Altamirano H.C. | |
dc.creator | Fritis, M.C. | |
dc.creator | Chamy M.C. | |
dc.date.accessioned | 2021-06-22T15:20:31Z | |
dc.date.accessioned | 2024-05-02T14:58:54Z | |
dc.date.available | 2021-06-22T15:20:31Z | |
dc.date.available | 2024-05-02T14:58:54Z | |
dc.date.created | 2021-06-22T15:20:31Z | |
dc.date.issued | 2007-12 | |
dc.identifier | MoleculesOpen AccessVolume 12, Issue 12, Pages 2605 - 2620December 2007 | |
dc.identifier | 1420-3049 | |
dc.identifier | http://repositorio.unab.cl/xmlui/handle/ria/19148 | |
dc.identifier | 10.3390/12122605 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/9260940 | |
dc.description.abstract | A route for the degradation of the side chain of ent-labdane derivatives has been devised, giving the useful synthon 2β,12-dihydroxy-13,14,15,16,17- pentanor-ent-labdane-8-one (8). The use of this compound in the preparation of terpenylquinone derivatives shall be reported elsewhere. In addition we have synthesized the compound 2β,12-diacetoxy-8β,17-epoxy-13,14,15,16- tetranor-ent-labdane (10), which upon catalytic epoxide ring opening in alkaline or acid media gave rise in all cases to the formation of tricyclic compounds. © 2007 by MDPI. | |
dc.language | en | |
dc.publisher | MDPI | |
dc.subject | Ent-labdanes | |
dc.subject | Selective degradations | |
dc.subject | Unsaturated side chain | |
dc.title | Oxidative degradations of the side chain of unsaturated Ent-labdanes. Part II | |
dc.type | Artículo |