| http://dbpedia.org/ontology/abstract
|
The divinylcyclopropane-cycloheptadiene re … The divinylcyclopropane-cycloheptadiene rearrangement is an organic chemical transformation that involves the isomerization of a 1,2-divinylcyclopropane into a cycloheptadiene or -triene. It is conceptually related to the Cope rearrangement, but has the advantage of a strong thermodynamic driving force due to the release of ring strain. This thermodynamic power is recently being considered as an alternative energy source.onsidered as an alternative energy source.
|
| http://dbpedia.org/ontology/thumbnail
|
http://commons.wikimedia.org/wiki/Special:FilePath/DVCgen.png?width=300 +
|
| http://dbpedia.org/ontology/wikiPageID
|
27333066
|
| http://dbpedia.org/ontology/wikiPageLength
|
11459
|
| http://dbpedia.org/ontology/wikiPageRevisionID
|
1083487161
|
| http://dbpedia.org/ontology/wikiPageWikiLink
|
http://dbpedia.org/resource/Wittig_reaction +
, http://dbpedia.org/resource/Brine +
, http://dbpedia.org/resource/Sodium_bicarbonate +
, http://dbpedia.org/resource/Ylide +
, http://dbpedia.org/resource/Thermal_decomposition +
, http://dbpedia.org/resource/Thiirane +
, http://dbpedia.org/resource/Category:Cyclopropanes +
, http://dbpedia.org/resource/Category:Organic_reactions +
, http://dbpedia.org/resource/Thiepine +
, http://dbpedia.org/resource/Aziridine +
, http://dbpedia.org/resource/Lithium_diisopropylamide +
, http://dbpedia.org/resource/Azepine +
, http://dbpedia.org/resource/File:DVCPScopeDir.png +
, http://dbpedia.org/resource/File:DVCPScopeElim.png +
, http://dbpedia.org/resource/File:DVCEnant.png +
, http://dbpedia.org/resource/File:DVCPScopeCP.png +
, http://dbpedia.org/resource/File:DVCTM.png +
, http://dbpedia.org/resource/Pentane +
, http://dbpedia.org/resource/Pyrroline +
, http://dbpedia.org/resource/File:DVCex.png +
, http://dbpedia.org/resource/File:DVCPScopeLi.png +
, http://dbpedia.org/resource/Magnesium_sulfate +
, http://dbpedia.org/resource/File:DVCSynth2.png +
, http://dbpedia.org/resource/File:DVCsynth3.png +
, http://dbpedia.org/resource/File:DV_Epoxide_Mechanism_Rearrangements.png +
, http://dbpedia.org/resource/File:DVCgen.png +
, http://dbpedia.org/resource/File:DVCsynth.png +
, http://dbpedia.org/resource/File:Divinyl-CycloPropane_Rearrangement.png +
, http://dbpedia.org/resource/Silyl_enol_ether +
, http://dbpedia.org/resource/Tetrahydrofuran +
, http://dbpedia.org/resource/Hexamethylphosphoramide +
, http://dbpedia.org/resource/Chloroform +
, http://dbpedia.org/resource/Infrared_spectroscopy +
, http://dbpedia.org/resource/Category:Rearrangement_reactions +
, http://dbpedia.org/resource/Cope_rearrangement +
, http://dbpedia.org/resource/Nuclear_magnetic_resonance_spectroscopy +
, http://dbpedia.org/resource/Vinylcyclopropane_rearrangement +
, http://dbpedia.org/resource/Eucarvone +
, http://dbpedia.org/resource/Colchicine +
|
| http://dbpedia.org/property/wikiPageUsesTemplate
|
http://dbpedia.org/resource/Template:Reflist +
|
| http://purl.org/dc/terms/subject
|
http://dbpedia.org/resource/Category:Organic_reactions +
, http://dbpedia.org/resource/Category:Rearrangement_reactions +
, http://dbpedia.org/resource/Category:Cyclopropanes +
|
| http://purl.org/linguistics/gold/hypernym
|
http://dbpedia.org/resource/Transformation +
|
| http://www.w3.org/ns/prov#wasDerivedFrom
|
http://en.wikipedia.org/wiki/Divinylcyclopropane-cycloheptadiene_rearrangement?oldid=1083487161&ns=0 +
|
| http://xmlns.com/foaf/0.1/depiction
|
http://commons.wikimedia.org/wiki/Special:FilePath/DVCPScopeDir.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/DVCPScopeElim.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/DVCEnant.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/DVCPScopeCP.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/DVCTM.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/DVCex.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/DVCPScopeLi.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/DVCSynth2.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/DVCsynth3.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/DVCgen.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/DVCsynth.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/DV_Epoxide_Mechanism_Rearrangements.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Divinyl-CycloPropane_Rearrangement.png +
|
| http://xmlns.com/foaf/0.1/isPrimaryTopicOf
|
http://en.wikipedia.org/wiki/Divinylcyclopropane-cycloheptadiene_rearrangement +
|
| owl:sameAs |
http://dbpedia.org/resource/Divinylcyclopropane-cycloheptadiene_rearrangement +
, http://www.wikidata.org/entity/Q5284403 +
, https://global.dbpedia.org/id/4jDNs +
, http://yago-knowledge.org/resource/Divinylcyclopropane-cycloheptadiene_rearrangement +
, http://rdf.freebase.com/ns/m.0by0j89 +
|
| rdf:type |
http://dbpedia.org/class/yago/GeneralAnesthetic103433434 +
, http://dbpedia.org/ontology/ProgrammingLanguage +
, http://dbpedia.org/class/yago/Substance100020090 +
, http://dbpedia.org/class/yago/CausalAgent100007347 +
, http://dbpedia.org/class/yago/Cyclopropane103155661 +
, http://dbpedia.org/class/yago/WikicatCyclopropanes +
, http://dbpedia.org/class/yago/ChemicalReaction113447361 +
, http://dbpedia.org/class/yago/WikicatOrganicReactions +
, http://dbpedia.org/class/yago/NaturalProcess113518963 +
, http://dbpedia.org/class/yago/InhalationAnesthetic103570838 +
, http://dbpedia.org/class/yago/Process100029677 +
, http://dbpedia.org/class/yago/ChemicalProcess113446390 +
, http://dbpedia.org/class/yago/PhysicalEntity100001930 +
, http://dbpedia.org/class/yago/Matter100020827 +
, http://dbpedia.org/class/yago/Anesthetic102710766 +
, http://dbpedia.org/class/yago/Drug103247620 +
, http://dbpedia.org/class/yago/Agent114778436 +
|
| rdfs:comment |
The divinylcyclopropane-cycloheptadiene re … The divinylcyclopropane-cycloheptadiene rearrangement is an organic chemical transformation that involves the isomerization of a 1,2-divinylcyclopropane into a cycloheptadiene or -triene. It is conceptually related to the Cope rearrangement, but has the advantage of a strong thermodynamic driving force due to the release of ring strain. This thermodynamic power is recently being considered as an alternative energy source.onsidered as an alternative energy source.
|
| rdfs:label |
Divinylcyclopropane-cycloheptadiene rearrangement
|
