Gan et al., 1991 - Google Patents
Synthesis of D-erythroascorbic acid from D-glucoseGan et al., 1991
- Document ID
- 2683581749824816344
- Author
- Gan L
- Seib P
- Publication year
- Publication venue
- Carbohydrate research
External Links
Snippet
Reaction of a 4: 1 mixture of d-ribono-and d-arabinono-1, 4-lactones with benzaldehyde and hydrochloric acid gave 59% crystalline 3, 4-O-benzylidene-d-ribono-1, 5-lactone. This acetal was oxidized with manganese dioxide in acetone to its 2-keto derivative (6) in 76% yield …
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 OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O 0 title abstract description 26
Classifications
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- C07H19/16—Purine radicals
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- C07D307/62—Three oxygen atoms, e.g. ascorbic acid
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