%0 Journal Article
%T 2,3-FUNCTIONALLY DIALKYL-1,4-BENZOHYDROQUINONE DIACETATE DERIVATIVES FROM CLEAVAGE OF EPOXIDES
%A MOLINARI
%A AURORA
%A OLIVA
%A ALFONSO
%A AGUILERA
%A NANET
%A MIGUEL DEL CORRAL
%A JOSE Ma
%A GORDALIZA
%A MARINA
%A CASTRO
%A Ma ANGELES
%A GARCIA-GRAVALOS
%A Ma DOLORES
%A SAN FELICIANO
%A ARTURO
%J Bolet¨ªn de la Sociedad Chilena de Qu¨ªmica
%D 2001
%I Scientific Electronic Library Online
%R 10.4067/S0366-16442001000100007
%X 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
%K quinones
%K myrcene
%K terpenylhydroquinones
%K oxidative cleavage
%K epoxides.
%U http://www.scielo.cl/scielo.php?script=sci_abstract&pid=S0366-16442001000100007&lng=en&nrm=iso&tlng=en