Site and stereoselectivity of the cyclopropanation of unsymmetrically substituted 1,3-dienes by the Simmons-Smith reaction.

dc.creatorGuerreiro, MC
dc.creatorSchuchardt, U
dc.date1996
dc.date2014-07-30T19:58:00Z
dc.date2015-11-26T16:57:07Z
dc.date2014-07-30T19:58:00Z
dc.date2015-11-26T16:57:07Z
dc.date.accessioned2018-03-28T23:44:39Z
dc.date.available2018-03-28T23:44:39Z
dc.identifierSynthetic Communications. Taylor & Francis Inc, v. 26, n. 9, n. 1793, n. 1800, 1996.
dc.identifier0039-7911
dc.identifierWOS:A1996UE95200021
dc.identifier10.1080/00397919608002620
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/74302
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/74302
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1277577
dc.descriptionIn the Simmons-Smith reaction, 1,3-dienes are preferentially cyclopropanated at the more electron-rich double bond to afford the trans-vinylcyclopropane; an allylic hydroxyl group increases the reactivity and directs the cyclopropanation to the adjacent double bond.
dc.description26
dc.description9
dc.description1793
dc.description1800
dc.languageen
dc.publisherTaylor & Francis Inc
dc.publisherPhiladelphia
dc.publisherEUA
dc.relationSynthetic Communications
dc.relationSynth. Commun.
dc.rightsfechado
dc.rightshttp://journalauthors.tandf.co.uk/permissions/reusingOwnWork.asp
dc.sourceWeb of Science
dc.titleSite and stereoselectivity of the cyclopropanation of unsymmetrically substituted 1,3-dienes by the Simmons-Smith reaction.
dc.typeArtículos de revistas


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