dc.creator | MOLINARI,AURORA | |
dc.creator | OLIVA,ALFONSO | |
dc.creator | AGUILERA,NANET | |
dc.creator | MIGUEL DEL CORRAL,JOSE Mª | |
dc.creator | GORDALIZA,MARINA | |
dc.creator | CASTRO,Mª ANGELES | |
dc.creator | GARCIA-GRAVALOS,Mª DOLORES | |
dc.creator | SAN FELICIANO,ARTURO | |
dc.date | 2001-03-01 | |
dc.date.accessioned | 2020-02-17T15:26:31Z | |
dc.date.available | 2020-02-17T15:26:31Z | |
dc.identifier | https://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0366-16442001000100007 | |
dc.identifier.uri | https://revistaschilenas.uchile.cl/handle/2250/126804 | |
dc.description | Several new 2,3-functionally dialkyl-1,4-benzohydroquinone diacetates have been prepared by oxidative cleavage of epoxide compounds III, obtained from the Diels-Alder condensation product between the monoterpene myrcene and 1,4-benzoquinone. The nature of the isolated products is depending of the functionality of the side chain | |
dc.format | text/html | |
dc.language | en | |
dc.publisher | Sociedad Chilena de Química | |
dc.relation | 10.4067/S0366-16442001000100007 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.source | Boletín de la Sociedad Chilena de Química v.46 n.1 2001 | |
dc.subject | Quinones | |
dc.subject | myrcene | |
dc.subject | terpenylhydroquinones | |
dc.subject | oxidative cleavage | |
dc.subject | epoxides | |
dc.title | 2,3-FUNCTIONALLY DIALKYL-1,4-BENZOHYDROQUINONE DIACETATE DERIVATIVES FROM CLEAVAGE OF EPOXIDES | |