Model reactions for electrophilic substitution of aromatic compounds
dc.contributor.author | Effenberger, Franz | de |
dc.date.accessioned | 2009-09-23 | de |
dc.date.accessioned | 2016-03-31T07:47:52Z | |
dc.date.available | 2009-09-23 | de |
dc.date.available | 2016-03-31T07:47:52Z | |
dc.date.issued | 1972 | de |
dc.date.updated | 2014-09-26 | de |
dc.description.abstract | Symmetrical 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.other | 316672459 | de |
dc.identifier.uri | http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-41970 | de |
dc.identifier.uri | http://elib.uni-stuttgart.de/handle/11682/1214 | |
dc.identifier.uri | http://dx.doi.org/10.18419/opus-1197 | |
dc.language.iso | en | de |
dc.rights | info:eu-repo/semantics/openAccess | de |
dc.subject.classification | Aromaten , Elektrophile Substitution | de |
dc.subject.ddc | 540 | de |
dc.title | Model reactions for electrophilic substitution of aromatic compounds | en |
dc.type | article | de |
ubs.fakultaet | Fakultät Chemie | de |
ubs.institut | Institut für Organische Chemie | de |
ubs.opusid | 4197 | de |
ubs.publikation.source | Angewandte Chemie, International edition 11 (1972), S. 61-62. URL http://dx.doi.org./10.1002/anie.197200612 | de |
ubs.publikation.typ | Zeitschriftenartikel | de |