2,3-FUNCTIONALLY DIALKYL-1,4-BENZOHYDROQUINONE DIACETATE DERIVATIVES FROM CLEAVAGE OF EPOXIDES

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 fu...

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Main Authors: MOLINARI,AURORA, OLIVA,ALFONSO, AGUILERA,NANET, MIGUEL DEL CORRAL,JOSE Mª, GORDALIZA,MARINA, CASTRO,Mª ANGELES, GARCIA-GRAVALOS,Mª DOLORES, SAN FELICIANO,ARTURO
Language:English
Published: Sociedad Chilena de Química 2001
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Online Access:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0366-16442001000100007
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Summary: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