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dc.contributor.authorMorcillo Martínez, Sara Patricia 
dc.date.accessioned2024-01-26T13:48:18Z
dc.date.available2024-01-26T13:48:18Z
dc.date.issued2019-10
dc.identifier.citationAngewandte Chemie International Edition 58 (40), 14044-14054es_ES
dc.identifier.urihttps://hdl.handle.net/10481/87399
dc.description.abstractJust as “Deconstructivism”appearedas anovel movement in archi-tecturein the 1980s,deconstructiveapproaches haverecentlyemergedas excellentstrategiesfor scaffoldhoppingmodificationsin chemistry.The deconstructionand functionalizationof cyclicmoleculesmainlyinvolvesthe cleavageof the carbon–carbon(C@C) bondfollowedbythe constructionof new bonds.The cleavageof inertC@Csinglebonds,especiallyin unstrainedcycles,and theirsubsequentfunctionalizationis still one of the mostsought-afterchallengesin chemistry.Inthis vein,radical-mediatedstrategiesprovidean excellentapproachforachievingthis aim.Thisminireviewis an outlineof the historyofhomolyticcleavageand highlightsthe recentadvancesin exploringnewchemicalspaceby deconstructivefunctionalization.es_ES
dc.description.sponsorshipMINECO for the IJCI-2017-31674 contract.es_ES
dc.language.isoenges_ES
dc.publisherWiley Online Libraryes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleRadical‐promoted C‐C bond cleavage: a deconstructive approach for selective functionalizationes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1002/anie.201905218
dc.type.hasVersionVoRes_ES


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