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On the formation of 2,3-dihydroxyacetophenone from pentoses or hexuronic acids

✍ Scribed by Tania Ahmad; Rolf Andersson; Kjell Olsson; Olof Theander


Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
229 KB
Volume
247
Category
Article
ISSN
0008-6215

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✦ Synopsis


The structure of a previously isolated intermediate in the title reaction has been revised to 3-acetyl-2,3,4-trihydroxycyclohexanone by high-field 'H NMR spectroscopy. The three hydroxyl groups are mutually c&related. * Corresponding author. + All chiral compounds were obtained as racemic mixtures, but only one enantiomer is shown.


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