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- Hofmann–Martius_rearrangement abstract "The Hofmann–Martius rearrangement in organic chemistry is a rearrangement reaction converting an N-alkylated aniline to the corresponding ortho and / or para aryl-alkylated aniline. The reaction requires heat, and the catalyst is an acid like hydrochloric acid.The Hofmann–Martius rearrangementWhen the catalyst is a metal halide the reaction is also called the Reilly–Hickinbottom rearrangement.The reaction is also known to work for aryl ethers and two conceptually related reactions are the Fries rearrangement and the Fischer–Hepp rearrangement. Its reaction mechanism centers around dissociation of the reactant with the positively charged organic residue R attacking the aniline ring in a Friedel–Crafts alkylation.In one study this rearrangement was applied to a 3-N(CH3)(C6H5)-2-oxindole:Hofmann–Martius rearrangement of 3-N-Aryl-2-oxindoles↑ ↑ ↑ ↑ ↑".
- Hofmann–Martius_rearrangement thumbnail Hofmann-MartiusRearrangement.png?width=300.
- Hofmann–Martius_rearrangement wikiPageID "6395766".
- Hofmann–Martius_rearrangement wikiPageLength "2474".
- Hofmann–Martius_rearrangement wikiPageOutDegree "19".
- Hofmann–Martius_rearrangement wikiPageRevisionID "664688366".
- Hofmann–Martius_rearrangement wikiPageWikiLink Aniline.
- Hofmann–Martius_rearrangement wikiPageWikiLink Arene_substitution_pattern.
- Hofmann–Martius_rearrangement wikiPageWikiLink Aromatic_hydrocarbon.
- Hofmann–Martius_rearrangement wikiPageWikiLink Catalysis.
- Hofmann–Martius_rearrangement wikiPageWikiLink Category:Rearrangement_reactions.
- Hofmann–Martius_rearrangement wikiPageWikiLink Fischer–Hepp_rearrangement.
- Hofmann–Martius_rearrangement wikiPageWikiLink Friedel–Crafts_reaction.
- Hofmann–Martius_rearrangement wikiPageWikiLink Fries_rearrangement.
- Hofmann–Martius_rearrangement wikiPageWikiLink Hofmann–Martius_rearrangement.
- Hofmann–Martius_rearrangement wikiPageWikiLink Hydrochloric_acid.
- Hofmann–Martius_rearrangement wikiPageWikiLink Organic_chemistry.
- Hofmann–Martius_rearrangement wikiPageWikiLink Reaction_mechanism.
- Hofmann–Martius_rearrangement wikiPageWikiLink Rearrangement_reaction.
- Hofmann–Martius_rearrangement wikiPageWikiLink File:Hofmann-MartiusApplication.png.
- Hofmann–Martius_rearrangement wikiPageWikiLink File:Hofmann-MartiusRearrangement.png.
- Hofmann–Martius_rearrangement wikiPageWikiLinkText "Hofmann–Martius rearrangement".
- Hofmann–Martius_rearrangement subject Category:Rearrangement_reactions.
- Hofmann–Martius_rearrangement hypernym Reaction.
- Hofmann–Martius_rearrangement type Disease.
- Hofmann–Martius_rearrangement type Eponym.
- Hofmann–Martius_rearrangement type Reaction.
- Hofmann–Martius_rearrangement type Redirect.
- Hofmann–Martius_rearrangement comment "The Hofmann–Martius rearrangement in organic chemistry is a rearrangement reaction converting an N-alkylated aniline to the corresponding ortho and / or para aryl-alkylated aniline.".
- Hofmann–Martius_rearrangement label "Hofmann–Martius rearrangement".
- Hofmann–Martius_rearrangement sameAs Q675525.
- Hofmann–Martius_rearrangement sameAs Hofmann-Martius-Umlagerung.
- Hofmann–Martius_rearrangement sameAs Penataan_ulang_Hofmann-Martius.
- Hofmann–Martius_rearrangement sameAs m.0g3tys.
- Hofmann–Martius_rearrangement sameAs Q675525.
- Hofmann–Martius_rearrangement sameAs Hofmann-Martius重排反应.
- Hofmann–Martius_rearrangement wasDerivedFrom Hofmann–Martius_rearrangement?oldid=664688366.
- Hofmann–Martius_rearrangement depiction Hofmann-MartiusRearrangement.png.
- Hofmann–Martius_rearrangement isPrimaryTopicOf Hofmann–Martius_rearrangement.