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A Kinetic Photometric Assay for the Quantification of the Open‐Chain Content of Aldoses

Aldoses exist predominantly in the cyclic hemiacetal form, which is in equilibrium with the open‐chain aldehyde form. The small aldehyde content hampers reactivity when chemistry addresses the carbonyl moiety. This low concentration of the available aldehyde is generally difficult to ascertain. Here...

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Detalles Bibliográficos
Autores principales: Kalaus, Hubert, Reichetseder, Alexander, Scheibelreiter, Verena, Rudroff, Florian, Stanetty, Christian, Mihovilovic, Marko D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252792/
https://www.ncbi.nlm.nih.gov/pubmed/34262391
http://dx.doi.org/10.1002/ejoc.202001641
Descripción
Sumario:Aldoses exist predominantly in the cyclic hemiacetal form, which is in equilibrium with the open‐chain aldehyde form. The small aldehyde content hampers reactivity when chemistry addresses the carbonyl moiety. This low concentration of the available aldehyde is generally difficult to ascertain. Herein, we demonstrate a new kinetic determination of the (minute) open‐chain content (OCC) of aldoses. This kinetic approach exploits the aldehyde‐selectivity of 2‐aminobenzamidoxime (ABAO), which furnishes a strongly UV‐active adduct. Simple formation curves can be measured in a photometer or plate reader for high‐throughput screening. Under pseudo‐first order kinetics, these curves correlate with a prediction model yielding the relative OCC. The OCCs of all parent aldoses (pentoses and hexoses) were determined referencing against the two tetroses with exceptionally high OCCs and were in very good agreement with literature data. Additionally, the assay was extended towards higher‐carbon sugars with unknown OCC and also applied to rationalise a lack of reactivity observed in a recent synthetic investigation.