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- Neber_rearrangement abstract "The Neber rearrangement is an organic reaction in which an oxime is converted into an alpha-aminoketone in a rearrangement reaction.Neber rearrangementThe oxime is first converted to a ketoxime tosylate by reaction with tosyl chloride. Added base forms a carbanion which displaces the tosylate group in a nucleophilic displacement to an azirine and added water subsequently hydrolyses it to the aminoketone.The Beckmann rearrangement is a side reaction.".
- Neber_rearrangement thumbnail NeberRearrangement.svg?width=300.
- Neber_rearrangement wikiPageID "15184100".
- Neber_rearrangement wikiPageLength "956".
- Neber_rearrangement wikiPageOutDegree "14".
- Neber_rearrangement wikiPageRevisionID "551724504".
- Neber_rearrangement wikiPageWikiLink 4-Toluenesulfonyl_chloride.
- Neber_rearrangement wikiPageWikiLink Azirine.
- Neber_rearrangement wikiPageWikiLink Base_(chemistry).
- Neber_rearrangement wikiPageWikiLink Beckmann_rearrangement.
- Neber_rearrangement wikiPageWikiLink Carbanion.
- Neber_rearrangement wikiPageWikiLink Category:Name_reactions.
- Neber_rearrangement wikiPageWikiLink Category:Rearrangement_reactions.
- Neber_rearrangement wikiPageWikiLink Nucleophilic_substitution.
- Neber_rearrangement wikiPageWikiLink Organic_reaction.
- Neber_rearrangement wikiPageWikiLink Oxime.
- Neber_rearrangement wikiPageWikiLink Rearrangement_reaction.
- Neber_rearrangement wikiPageWikiLink Side_reaction.
- Neber_rearrangement wikiPageWikiLink Tosyl.
- Neber_rearrangement wikiPageWikiLink File:NeberRearrangement.svg.
- Neber_rearrangement wikiPageWikiLinkText "Neber rearrangement".
- Neber_rearrangement wikiPageUsesTemplate Template:Reflist.
- Neber_rearrangement subject Category:Name_reactions.
- Neber_rearrangement subject Category:Rearrangement_reactions.
- Neber_rearrangement hypernym Reaction.
- Neber_rearrangement type Disease.
- Neber_rearrangement type Eponym.
- Neber_rearrangement type Reaction.
- Neber_rearrangement comment "The Neber rearrangement is an organic reaction in which an oxime is converted into an alpha-aminoketone in a rearrangement reaction.Neber rearrangementThe oxime is first converted to a ketoxime tosylate by reaction with tosyl chloride. Added base forms a carbanion which displaces the tosylate group in a nucleophilic displacement to an azirine and added water subsequently hydrolyses it to the aminoketone.The Beckmann rearrangement is a side reaction.".
- Neber_rearrangement label "Neber rearrangement".
- Neber_rearrangement sameAs Q904114.
- Neber_rearrangement sameAs إعادة_ترتيب_نيبر.
- Neber_rearrangement sameAs Neber-Umlagerung.
- Neber_rearrangement sameAs Transposición_de_Neber.
- Neber_rearrangement sameAs Penataan_ulang_Neber.
- Neber_rearrangement sameAs ネバー転位.
- Neber_rearrangement sameAs Przegrupowanie_Nebera.
- Neber_rearrangement sameAs m.03hl66p.
- Neber_rearrangement sameAs Перегруппировка_Небера.
- Neber_rearrangement sameAs Q904114.
- Neber_rearrangement sameAs 内博重排反应.
- Neber_rearrangement wasDerivedFrom Neber_rearrangement?oldid=551724504.
- Neber_rearrangement depiction NeberRearrangement.svg.
- Neber_rearrangement isPrimaryTopicOf Neber_rearrangement.