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dc.creatorMOLINARI,AURORA
dc.creatorOLIVA,ALFONSO
dc.creatorAGUILERA,NANET
dc.creatorMIGUEL DEL CORRAL,JOSE Mª
dc.creatorGORDALIZA,MARINA
dc.creatorCASTRO,Mª ANGELES
dc.creatorGARCIA-GRAVALOS,Mª DOLORES
dc.creatorSAN FELICIANO,ARTURO
dc.date2001-03-01
dc.date.accessioned2019-09-10T12:40:14Z
dc.date.available2019-09-10T12:40:14Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0366-16442001000100007
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/105714
dc.descriptionSeveral 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.formattext/html
dc.languageen
dc.publisherSociedad Chilena de Química
dc.relation10.4067/S0366-16442001000100007
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceBoletín de la Sociedad Chilena de Química v.46 n.1 2001
dc.subjectQuinones
dc.subjectmyrcene
dc.subjectterpenylhydroquinones
dc.subjectoxidative cleavage
dc.subjectepoxides
dc.title2,3-FUNCTIONALLY DIALKYL-1,4-BENZOHYDROQUINONE DIACETATE DERIVATIVES FROM CLEAVAGE OF EPOXIDES


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