A convenient preparation of 1,2,3,4,5,6,7,8-octahydro-naphthalene skeleton. Synthesis of (+/-)-isocaridiene

dc.creatorImamura, PM
dc.creatorCosta, M
dc.creatorCustodio, R
dc.date2002
dc.date2014-11-19T04:37:00Z
dc.date2015-11-26T17:02:10Z
dc.date2014-11-19T04:37:00Z
dc.date2015-11-26T17:02:10Z
dc.date.accessioned2018-03-28T23:50:13Z
dc.date.available2018-03-28T23:50:13Z
dc.identifierSynthetic Communications. Marcel Dekker Inc, v. 32, n. 9, n. 1393, n. 1399, 2002.
dc.identifier0039-7911
dc.identifierWOS:000175809600013
dc.identifier10.1081/SCC-120003636
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/53035
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/53035
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/53035
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1278863
dc.descriptionSynthesis of isocaridiene, an isomeric compound of natural sesquiterpene caridiene, is described starting from myrcene. Dehydration of tertiary alcohol leading exclusively to isocaridiene was in agreement with the semiempirical and ab initio quantum mechanical calculations.
dc.description32
dc.description9
dc.description1393
dc.description1399
dc.languageen
dc.publisherMarcel Dekker Inc
dc.publisherNew York
dc.publisherEUA
dc.relationSynthetic Communications
dc.relationSynth. Commun.
dc.rightsfechado
dc.sourceWeb of Science
dc.subjectSesquiterpene
dc.subjectNanaimoal
dc.titleA convenient preparation of 1,2,3,4,5,6,7,8-octahydro-naphthalene skeleton. Synthesis of (+/-)-isocaridiene
dc.typeArtículos de revistas


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