Ascorbic acid relationship between dehydroascorbic

The structure of 138 was elucidated, shortly after its isolation, in extensive contributions by many groups. Several important discoveries relating to its constitution were reported in 1933, the same year in which the first successful synthesis was described (see Refs. 274, 324). Thus, the group at the University of Birmingham335 found that the primary oxidation product of 138, the 2,3-diulosono-lactone 148 (dehydroascorbic acid), could be quantitatively oxidized by sodium hypoiodite to generate oxalic acid and L-threonic acid (Scheme 16), which was identified as the crystalline tri-O-methyl-L-threonamide. These results established the stereochemical relationship between 138 and L-gulonic (and L-idonic) acid. The work that provided support for the structure of L-ascorbic acid has been summarized in several reviews.274,336... 

The relationship between ascorbic acid and dehydroascorbic acid on the rate of strawberry pigment loss in water-soluble pigment (St B) is given graphically in Figure 6. 

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