The Composition of Keto Aldoses in Aqueous Solution as Determined by NMR Spectroscopy

Abstract

Abstract Keto aldoses usually form complex mixtures of equilibrating isomers in solution. This is due to the two different positions that may be used for ring closure in dicarbonyl sugars. The composition of various 2‐keto aldoses 1 – 5 and 8 , the 3‐keto aldose 2‐deoxy‐ D ‐ erythro ‐hexos‐3‐ulose ( 9 ), and the ketose 1‐deoxy‐ D ‐ribulose ( 10 ) in aqueous solution has been determined by NMR spectroscopy. The investigated keto aldoses form equilibria containing three to fifteen isomers. Among various furanose and pyranose ring structures stemming from 1,4‐, 1,5‐, 2,5‐, and 2,6‐cyclization, bicyclic forms were also found in several cases. The 2‐keto aldoses mainly exist as hydrated isomers in H 2 O. Therefore, these forms and their proportions were compared to forms found in two homomorphous aldoses and one homomorphous ketose as model compounds. Besides the NMR data, also the composition of the 2‐keto aldoses agreed with the average of forms found in the model compounds, a finding that might eventually be useful for deducing the composition of other keto aldoses.