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http://dx.doi.org/10.18419/opus-997
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DC Element | Wert | Sprache |
---|---|---|
dc.contributor.author | Effenberger, Franz | de |
dc.contributor.author | Podszun, Wolfgang | de |
dc.date.accessioned | 2009-07-22 | de |
dc.date.accessioned | 2016-03-31T07:47:24Z | - |
dc.date.available | 2009-07-22 | de |
dc.date.available | 2016-03-31T07:47:24Z | - |
dc.date.issued | 1969 | de |
dc.identifier.other | 314611665 | de |
dc.identifier.uri | http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-41828 | de |
dc.identifier.uri | http://elib.uni-stuttgart.de/handle/11682/1014 | - |
dc.identifier.uri | http://dx.doi.org/10.18419/opus-997 | - |
dc.description.abstract | While the stabilization of cationic centers by alpha cyclopropyl groups has been verified in many instances [2,31, to the best of our knowledge nothing is known about the influenceof cyclopropyl groups, as substituents, on the reaction mechanism of multiple bonds. The α-cyclopropylcarbonium ions 141 that may be formed are capable of rearrangement, thus providing additional information as to a polar or a more concerted mechanism of cycloaddition. | en |
dc.language.iso | en | de |
dc.rights | info:eu-repo/semantics/openAccess | de |
dc.subject.classification | Cycloaddition , Ethylen | de |
dc.subject.ddc | 540 | de |
dc.title | Cycloadditions to 1,1-Dicyclopropylethylene | en |
dc.type | article | de |
dc.date.updated | 2014-09-26 | de |
ubs.fakultaet | Fakultät Chemie | de |
ubs.institut | Institut für Organische Chemie | de |
ubs.opusid | 4182 | de |
ubs.publikation.source | Angewandte Chemie, International edition 8 (1969), S. 976. URL http://dx.doi.org./10.1002/anie.196909761 | de |
ubs.publikation.typ | Zeitschriftenartikel | de |
Enthalten in den Sammlungen: | 03 Fakultät Chemie |
Dateien zu dieser Ressource:
Datei | Beschreibung | Größe | Format | |
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eff73.pdf | 276,71 kB | Adobe PDF | Öffnen/Anzeigen |
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