Model reactions for electrophilic substitution of aromatic compounds

dc.contributor.authorEffenberger, Franzde
dc.date.accessioned2009-09-23de
dc.date.accessioned2016-03-31T07:47:52Z
dc.date.available2009-09-23de
dc.date.available2016-03-31T07:47:52Z
dc.date.issued1972de
dc.date.updated2014-09-26de
dc.description.abstractSymmetrical triaminobenzenes are particularly suitable as model compounds for studying electrophilic aromatic reactions; due to the additive electron releasing influence of three mutually meta dialkylamino groups in (1), cationic intermediates are stabilized to such a degree that individual steps of electrophilic substitution can separately studied.en
dc.identifier.other316672459de
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-41970de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/1214
dc.identifier.urihttp://dx.doi.org/10.18419/opus-1197
dc.language.isoende
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.subject.classificationAromaten , Elektrophile Substitutionde
dc.subject.ddc540de
dc.titleModel reactions for electrophilic substitution of aromatic compoundsen
dc.typearticlede
ubs.fakultaetFakultät Chemiede
ubs.institutInstitut für Organische Chemiede
ubs.opusid4197de
ubs.publikation.sourceAngewandte Chemie, International edition 11 (1972), S. 61-62. URL http://dx.doi.org./10.1002/anie.197200612de
ubs.publikation.typZeitschriftenartikelde

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