Synthesis of 5-amino-5-deoxy-d-mannopyranose and 1,5-di-deoxy-1,5-imino-d-mannitol, and inhibition of α- and β-d-mannosidases
✍ Scribed by Günter Legler; Elisabeth Jülich
- Book ID
- 107725407
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 772 KB
- Volume
- 128
- Category
- Article
- ISSN
- 0008-6215
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📜 SIMILAR VOLUMES
By an Amadori rearrangement of easily available 5-azido-5-deoxy-D-glucofuranose with dibenzylamine and subsequent catalytic hydrogenation of the resulting 5-azido-l-dibenzylamino-l,5dideoxy-D-fructopyranose, the new l-amino-l,2,5-trideoxy-2,5-ilnino-D-mannitol was obtained in only two steps and exce
The syntheses have been described of the 2-acetamido-2-deoxy derivatives of 5-thio-D-glucose lm3, 5-thio-D-mannose 4, 5-thio-D-allose 5, 3-acetamido-3-deoxy5thio-D-xylose6, and 4-acetamido-4-deoxy-5-thio-r\_-lyxose6. We now report the syntheses of 3-amino-3-deoxy-5-thio-D-allose hydrochloride and a