Abstract
The two
3-deoxy-D-hexosones, 3-deoxy-D-erythrohexosone and 3-deoxy-D-threohexosone, were
quantitatively converted by acid to 5-(hydroxymethyl)-2-furaldehyde.The
mechanism of the formation of 2-furaldehyde from sugars is discussed.
Calcium hydroxide
rapidly converted 3-deoxy-D-erythrohexosone to α- and β-glucometasaccharinic
acids, and 3-deoxy-D-threohexosone to α- and β-galactometasaccharinic
acids.
Cited by
46 articles.
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