dc.contributorAckermann, Lutz
dc.creatorVaillard, Santiago Eduardo
dc.creatorSchulte, Birte
dc.creatorStuder, Armido
dc.date.accessioned2020-08-26T16:01:24Z
dc.date.accessioned2022-10-15T12:57:28Z
dc.date.available2020-08-26T16:01:24Z
dc.date.available2022-10-15T12:57:28Z
dc.date.created2020-08-26T16:01:24Z
dc.date.issued2009
dc.identifierVaillard, Santiago Eduardo; Schulte, Birte; Studer, Armido; Radical Based Arylation Methods; Wiley; 2009; 475-511
dc.identifier978-3-527-31937-4
dc.identifierhttp://hdl.handle.net/11336/112465
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4388678
dc.description.abstractMost of the radical reactions can be conducted under mild conditions. In contrast to ionic reactions and many transition-metal mediated processes most of the functional groups are tolerated under radical conditions. Moreover, radical reactions can be performed in various solvents; even water is tolerated as a reaction medium. These facts among others make radical processes highly useful for arylations. Radical arylations can be performed by SRN1 type reactions, by homolytic aromatic substitutions, and by reactions of aryl radicals with various radical acceptors. In the present book article we first focus on SRN1 type reactions .
dc.languageeng
dc.publisherWiley
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.wiley.com/en-us/Modern+Arylation+Methods-p-9783527319374
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.sourceModern Arylation Methods
dc.subjectARYLATION REACTION
dc.subjectHOMOLYTIC SUBSTITUTION
dc.subjectARYL RADICALS
dc.subjectRADICAL CHEMISTRY
dc.titleRadical Based Arylation Methods
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typeinfo:eu-repo/semantics/bookPart
dc.typeinfo:ar-repo/semantics/parte de libro


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