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.[1] The reaction is important in carbohydrate chemistry, specifically the glycation of hemoglobin (as measured by the HbA1c test).[2]
The rearrangement is usually preceded by formation of a α-hydroxyimine by condensation of an amine with an aldose sugar. The rearrangement itself entails intramolecular redox reaction, converting this α-hydroxyimine to an α-ketoamine:
The formation of imines is generally reversible, but subsequent to conversion to the keto-amine, the attached amine is fixed irreversibly. This Amadori product is an intermediate in the production of advanced glycation end-products (AGE)s. The formation of an advanced glycation end-product involves the oxidation of the Amadori product.
YouTube Encyclopedic
-
1/5Views:1 64721 817430114 41877 813
-
Osazone Formation | Amadori Rearrangement | Weygand Mechanism
-
Osazone formation mechanism
-
How to say Amadori rearrangement in German?
-
What is the Maillard Reaction - Food Science
-
Osazone Formation test|Kiliani fischer synthesis|Ruff Degradation|Chain Shortening Elongation
Transcription
Food chemistry
The reaction is associated with the amino-carbonyl reactions (also called glycation reaction, or Maillard reaction)[3] in which the reagents are naturally occurring sugars and amino acids. One study demonstrated the possibility of Amadori rearrangement during interaction between oxidized dextran and gelatine.[4]
History
The Amadori rearrangement was discovered by the organic chemist Mario Amadori (1886–1941), who in 1925 reported this reaction while studying the Maillard reaction.[5][6]
See also
- Fructoselysine, the Amadori product derived from glucose and lysine
- Glycated hemoglobin, the Amadori product used in the HbA1c diagnostic test for diabetes
References
- ^ Strategic Applications of Named Reactions in Organic Synthesis (Paperback) by Laszlo Kurti, BN 0-12-429785-4
- ^ Koenig, R. J.; Cerami, A. (1980). "Hemoglobin A Ic and diabetes mellitus". Annual Review of Medicine. 31: 29–34. doi:10.1146/annurev.me.31.020180.000333. PMID 6994614.
- ^ This vo Kientza, Hervé. "IMARS Highligh". www.imarsonline.com/.
- ^ Berillo, Dmitriy; Natalia Volkova (2014). "Preparation and physicochemical characteristics of cryogel based on gelatin and oxidised dextran". Journal of Materials Science. 49 (14): 4855–4868. Bibcode:2014JMatS..49.4855B. doi:10.1007/s10853-014-8186-3. S2CID 96843083.
- ^ M. Amadori, Atti. reale accad. nazl. Lincei, [6] 2, 337 (1925); [6] 9, 68, 226 (1929); [6] 13, 72 (1931)
- ^ Strategic Applications of Named Reactions in Organic Synthesis (Paperback) by Laszlo Kurti, BN 0-12-429785-4
External links
- Amadori Rearrangement, PowerPoint presentation detailing the reaction mechanism
This page was last edited on 19 November 2023, at 13:54