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vol.46 issue1CHEMICAL-MICROBIOLOGICAL SYNTHESIS OF PROGESTERONEEXTRACTION OF POLYFLAVONOIDS FROM Pinus radiata D. Don BARK: EVALUATION OF EFFECTS OF SOLVENT COMPOSITION AND OF THE HEIGHT ON TREE BARK author indexsubject indexarticles search
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Boletín de la Sociedad Chilena de Química

Print version ISSN 0366-1644

Abstract

MOLINARI, AURORA et al. 2,3-FUNCTIONALLY DIALKYL-1,4-BENZOHYDROQUINONE DIACETATE DERIVATIVES FROM CLEAVAGE OF EPOXIDES. Bol. Soc. Chil. Quím. [online]. 2001, vol.46, n.1, pp.33-39. ISSN 0366-1644.  http://dx.doi.org/10.4067/S0366-16442001000100007.

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

Keywords : Quinones; myrcene; terpenylhydroquinones; oxidative cleavage; epoxides.

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