Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Amadori_rearrangement> ?p ?o }
Showing triples 1 to 77 of
77
with 100 triples per page.
- Amadori_rearrangement abstract "The Amadori rearrangement is an organic reaction describing the acid or base catalyzed isomerization or rearrangement reaction of the N-glycoside of an aldose or the glycosylamine to the corresponding 1-amino-1-deoxy-ketose. The reaction is important in carbohydrate chemistry.The reaction mechanism is demonstrated starting from the reaction of D-mannose in its closed (1) and open-form (2) with ammonia to produce the 1,1-amino-alcohol (3), which is unstable and loses water to the glycosylamine (again the open imine (5) and the closed form hemiaminal (4)), which is the starting point for the actual Amadori rearrangement.By treatment of the glycosylamine with pyridine and acetic anhydride, the imine group rearranges and the intermediate enol, in turn, rearranges to the ketone. In this particular reaction, all the alcohol and amino groups are acylated as well.The reaction is associated with the Maillard reaction in which the reagents are naturally occurring sugars and amino acids. Recent study is revealed the possibility of Amadori rearrangement during interaction between oxidized dextran and gelatine.".
- Amadori_rearrangement thumbnail AmadoriRearrangement1.png?width=300.
- Amadori_rearrangement wikiPageExternalLink amadori_rearrangement.ppt.
- Amadori_rearrangement wikiPageID "7668353".
- Amadori_rearrangement wikiPageLength "3903".
- Amadori_rearrangement wikiPageOutDegree "49".
- Amadori_rearrangement wikiPageRevisionID "699794843".
- Amadori_rearrangement wikiPageWikiLink Acetic_anhydride.
- Amadori_rearrangement wikiPageWikiLink Acid_catalysis.
- Amadori_rearrangement wikiPageWikiLink Acylation.
- Amadori_rearrangement wikiPageWikiLink Advanced_glycation_end-product.
- Amadori_rearrangement wikiPageWikiLink Alcohol.
- Amadori_rearrangement wikiPageWikiLink Aldehyde.
- Amadori_rearrangement wikiPageWikiLink Aldose.
- Amadori_rearrangement wikiPageWikiLink Amine.
- Amadori_rearrangement wikiPageWikiLink Amino_acid.
- Amadori_rearrangement wikiPageWikiLink Ammonia.
- Amadori_rearrangement wikiPageWikiLink Atom.
- Amadori_rearrangement wikiPageWikiLink Carbohydrate_chemistry.
- Amadori_rearrangement wikiPageWikiLink Carbon.
- Amadori_rearrangement wikiPageWikiLink Catalysis.
- Amadori_rearrangement wikiPageWikiLink Category:Name_reactions.
- Amadori_rearrangement wikiPageWikiLink Category:Posttranslational_modification.
- Amadori_rearrangement wikiPageWikiLink Category:Rearrangement_reactions.
- Amadori_rearrangement wikiPageWikiLink Covalent_bond.
- Amadori_rearrangement wikiPageWikiLink Deoxygenation.
- Amadori_rearrangement wikiPageWikiLink Enol.
- Amadori_rearrangement wikiPageWikiLink Fructoselysine.
- Amadori_rearrangement wikiPageWikiLink Glucose.
- Amadori_rearrangement wikiPageWikiLink Glycation.
- Amadori_rearrangement wikiPageWikiLink Glycoside.
- Amadori_rearrangement wikiPageWikiLink Glycosylamine.
- Amadori_rearrangement wikiPageWikiLink Hemiaminal.
- Amadori_rearrangement wikiPageWikiLink Hydrogen.
- Amadori_rearrangement wikiPageWikiLink Hydroxyl.
- Amadori_rearrangement wikiPageWikiLink Imine.
- Amadori_rearrangement wikiPageWikiLink Isomerization.
- Amadori_rearrangement wikiPageWikiLink Ketone.
- Amadori_rearrangement wikiPageWikiLink Ketose.
- Amadori_rearrangement wikiPageWikiLink Lysine.
- Amadori_rearrangement wikiPageWikiLink Maillard_reaction.
- Amadori_rearrangement wikiPageWikiLink Mannose.
- Amadori_rearrangement wikiPageWikiLink Nitrogen.
- Amadori_rearrangement wikiPageWikiLink Organic_reaction.
- Amadori_rearrangement wikiPageWikiLink Protein.
- Amadori_rearrangement wikiPageWikiLink Pyridine.
- Amadori_rearrangement wikiPageWikiLink Reaction_mechanism.
- Amadori_rearrangement wikiPageWikiLink Rearrangement_reaction.
- Amadori_rearrangement wikiPageWikiLink Schiff_base.
- Amadori_rearrangement wikiPageWikiLink Transition_metal.
- Amadori_rearrangement wikiPageWikiLink File:AmadoriRearrangement1.png.
- Amadori_rearrangement wikiPageWikiLinkText "Amadori adduct".
- Amadori_rearrangement wikiPageWikiLinkText "Amadori reactions".
- Amadori_rearrangement wikiPageWikiLinkText "Amadori rearrangement".
- Amadori_rearrangement wikiPageWikiLinkText "rearranges".
- Amadori_rearrangement wikiPageUsesTemplate Template:Reflist.
- Amadori_rearrangement subject Category:Name_reactions.
- Amadori_rearrangement subject Category:Posttranslational_modification.
- Amadori_rearrangement subject Category:Rearrangement_reactions.
- Amadori_rearrangement hypernym Reaction.
- Amadori_rearrangement type Disease.
- Amadori_rearrangement type Eponym.
- Amadori_rearrangement type Reaction.
- Amadori_rearrangement comment "The Amadori rearrangement is an organic reaction describing the acid or base catalyzed isomerization or rearrangement reaction of the N-glycoside of an aldose or the glycosylamine to the corresponding 1-amino-1-deoxy-ketose.".
- Amadori_rearrangement label "Amadori rearrangement".
- Amadori_rearrangement sameAs Q452196.
- Amadori_rearrangement sameAs Amadori-Umlagerung.
- Amadori_rearrangement sameAs Transposición_de_Amadori.
- Amadori_rearrangement sameAs Riarrangiamento_di_Amadori.
- Amadori_rearrangement sameAs アマドリ転位.
- Amadori_rearrangement sameAs m.0268cg3.
- Amadori_rearrangement sameAs Перегруппировка_Амадори.
- Amadori_rearrangement sameAs Q452196.
- Amadori_rearrangement sameAs 阿马道里重排.
- Amadori_rearrangement wasDerivedFrom Amadori_rearrangement?oldid=699794843.
- Amadori_rearrangement depiction AmadoriRearrangement1.png.
- Amadori_rearrangement isPrimaryTopicOf Amadori_rearrangement.