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- Wagner–Meerwein_rearrangement abstract "A Wagner–Meerwein rearrangement is a class of carbocation 1,2-rearrangement reactions in which a hydrogen, alkyl or aryl group migrates from one carbon to a neighboring carbon.Several reviews have been published.The rearrangement was first discovered in bicyclic terpenes for example the conversion of isoborneol to camphene:The story of the rearrangement reveals that many scientists were puzzled with this and related reactions and its close relationship to the discovery of carbocations as intermediates.In a simple demonstration reaction of 1,4-dimethoxybenzene with either 2-methyl-2-butanol or 3-methyl-2-butanol in sulfuric acid and acetic acid yields the same disubstituted product, the latter via a hydride shift of the cationic intermediate:Carbocation rearrangement Polito 2010Currently, there are works relating to the use of skeletal rearrangement in the synthesis of bridged azaheterocycles. These data are summarized in 950pxPlausible mechanisms of the Wagner–Meerwein rearrangement of diepoxyisoindoles:1000pxThe related Nametkin rearrangement named after Sergey Namyotkin involves the rearrangement of methyl groups in certain terpenes. In some cases the reaction type is also called a retropinacol rearrangement (see Pinacol rearrangement).".
- Wagner–Meerwein_rearrangement thumbnail Wagner-Meerwein_Camphen_mechanism.svg?width=300.
- Wagner–Meerwein_rearrangement wikiPageID "3055861".
- Wagner–Meerwein_rearrangement wikiPageLength "4579".
- Wagner–Meerwein_rearrangement wikiPageOutDegree "25".
- Wagner–Meerwein_rearrangement wikiPageRevisionID "704202824".
- Wagner–Meerwein_rearrangement wikiPageWikiLink 1,2-rearrangement.
- Wagner–Meerwein_rearrangement wikiPageWikiLink 1,4-Dimethoxybenzene.
- Wagner–Meerwein_rearrangement wikiPageWikiLink 3-Methyl-2-butanol.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Acetic_acid.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Alkyl.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Aryl.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Bicyclic_molecule.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Borneol.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Camphene.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Carbocation.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Category:Name_reactions.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Category:Rearrangement_reactions.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Demjanov_rearrangement.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Hydrogen.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Pinacol_rearrangement.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Rearrangement_reaction.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Sergey_Namyotkin.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Sulfuric_acid.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Terpene.
- Wagner–Meerwein_rearrangement wikiPageWikiLink Tert-Amyl_alcohol.
- Wagner–Meerwein_rearrangement wikiPageWikiLink File:Carbocation_rearrangement_polito_2010.svg.
- Wagner–Meerwein_rearrangement wikiPageWikiLink File:Wagner-Meerwein_Camphen_mechanism.svg.
- Wagner–Meerwein_rearrangement wikiPageWikiLink File:Wagner-Meerwein_rearrangement_of_diepoxyisoindoles.svg.
- Wagner–Meerwein_rearrangement wikiPageWikiLink File:Первая_схема.svg.
- Wagner–Meerwein_rearrangement wikiPageWikiLinkText "1,2-migration".
- Wagner–Meerwein_rearrangement wikiPageWikiLinkText "Wagner–Meerwein rearrangement".
- Wagner–Meerwein_rearrangement wikiPageUsesTemplate Template:Reflist.
- Wagner–Meerwein_rearrangement subject Category:Name_reactions.
- Wagner–Meerwein_rearrangement subject Category:Rearrangement_reactions.
- Wagner–Meerwein_rearrangement hypernym Carbocation.
- Wagner–Meerwein_rearrangement type Eponym.
- Wagner–Meerwein_rearrangement type Reaction.
- Wagner–Meerwein_rearrangement type Redirect.
- Wagner–Meerwein_rearrangement comment "A Wagner–Meerwein rearrangement is a class of carbocation 1,2-rearrangement reactions in which a hydrogen, alkyl or aryl group migrates from one carbon to a neighboring carbon.Several reviews have been published.The rearrangement was first discovered in bicyclic terpenes for example the conversion of isoborneol to camphene:The story of the rearrangement reveals that many scientists were puzzled with this and related reactions and its close relationship to the discovery of carbocations as intermediates.In a simple demonstration reaction of 1,4-dimethoxybenzene with either 2-methyl-2-butanol or 3-methyl-2-butanol in sulfuric acid and acetic acid yields the same disubstituted product, the latter via a hydride shift of the cationic intermediate:Carbocation rearrangement Polito 2010Currently, there are works relating to the use of skeletal rearrangement in the synthesis of bridged azaheterocycles. ".
- Wagner–Meerwein_rearrangement label "Wagner–Meerwein rearrangement".
- Wagner–Meerwein_rearrangement sameAs Q902347.
- Wagner–Meerwein_rearrangement sameAs Wagner-Meerwein-Umlagerung.
- Wagner–Meerwein_rearrangement sameAs Transposición_de_Wagner-Meerwein.
- Wagner–Meerwein_rearrangement sameAs Wagner–Meerwein-toisiintuminen.
- Wagner–Meerwein_rearrangement sameAs Réarrangement_de_Wagner-Meerwein.
- Wagner–Meerwein_rearrangement sameAs ワーグナー・メーヤワイン転位.
- Wagner–Meerwein_rearrangement sameAs Wagner-Meerwein-omlegging.
- Wagner–Meerwein_rearrangement sameAs Rearranjo_de_Wagner-Meerwein.
- Wagner–Meerwein_rearrangement sameAs m.08nklv.
- Wagner–Meerwein_rearrangement sameAs Перегруппировка_Вагнера_—_Меервейна.
- Wagner–Meerwein_rearrangement sameAs Q902347.
- Wagner–Meerwein_rearrangement sameAs 瓦格纳-梅尔外因重排反应.
- Wagner–Meerwein_rearrangement wasDerivedFrom Wagner–Meerwein_rearrangement?oldid=704202824.
- Wagner–Meerwein_rearrangement depiction Wagner-Meerwein_Camphen_mechanism.svg.
- Wagner–Meerwein_rearrangement isPrimaryTopicOf Wagner–Meerwein_rearrangement.