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The reaction of 3-deoxy-d-glycero-pentos-2-ulose (“3-deoxyxylosone”) with aminoguanidine

✍ Scribed by Jan Hirsch; John W. Bayness; James A. Blackledge; Milton S. Feather


Book ID
107726035
Publisher
Elsevier Science
Year
1991
Tongue
English
Weight
203 KB
Volume
220
Category
Article
ISSN
0008-6215

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📜 SIMILAR VOLUMES


3-Deoxy-l-glycero-pentos-2-ulose (3-deox
✍ Dong Bum Shin; Milton S. Feather 📂 Article 📅 1990 🏛 Elsevier Science 🌐 English ⚖ 287 KB

In acidic solution, L-ascorbic acid undergoes decarboxylation with the formation of 2-furancarbaldehyde, suggesting that a five-carbon fragment is probably produced as an intermediate in the reaction. Isbell' proposed 3-deoxy-L-glycero-pentos-2-ulose (3-deoxy+xylosone, 1) as a reaction intermediate.

The oxidation of 3-deoxy-d-erythro-hexos
✍ Michael A. Madson; Milton S. Feather 📂 Article 📅 1983 🏛 Elsevier Science 🌐 English ⚖ 273 KB

## Note The oxidation of 3-deoxy-D-erythro-hexos-2-ulose ("3-deoxyglucosone") to 3deoxy-D-erythro-2-hexulosonic acid ("2-keto-3-deoxy-D-gluconate") by D-glucase oxidase" 3-Deoxy-D-erJ,t/zro-3-hexulosonic acid ("2-heto-3-deoxy-D-glucollic acid", 2) is a bacterial metabolite that may arise from D-gl