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dc.creatorZárraga O.,Miguel
dc.creatorMiranda M.,Alberto
dc.date2003-06-01
dc.date.accessioned2019-11-14T12:57:05Z
dc.date.available2019-11-14T12:57:05Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0717-97072003000200007
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/118095
dc.descriptionThe modification of camphor at C(3) by an aldolization reaction using decanal followed by oxidation of the alcohols mixture was studied. The oxidation of the alcohols mixture with sodium hypochlorite in pure ethanoic acid produces only 3-a-chloro-3-exo-decanoyl-1,7,7-trimethyl bicyclo[2.2.1]heptan-2-one
dc.formattext/html
dc.languageen
dc.publisherSociedad Chilena de Química
dc.relation10.4067/S0717-97072003000200007
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceJournal of the Chilean Chemical Society v.48 n.2 2003
dc.titleSTEREOSELECTIVE SYNTHESIS OF 3-alpha-CHLORO-3-EXO-DECANOYL CAMPHOR


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