The deamination of 2-amino-1,5-anhydro-2-deoxy-D-mannitol: hydride shift versus elimination
β Scribed by J.A. Ballantine; G. Hutchinson; J.Michael Williams
- Book ID
- 108308421
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- English
- Weight
- 183 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0008-6215
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π SIMILAR VOLUMES
Nucleoside analogues containing a 2-deoxy-l,5-anhydro-D-mannitol and a pyrimidine base moiety were synthesized starting from D-glucose via a nucleophilie opening of an epoxide with the heterocyelic base and an inversion of configuration at the 3'-position. Study of the conformation of these molecule
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
Enantiomerically pure 7-OxdbiCyClO[2.2.I]hept-5-en-2-yl derivatives ('naked sugars') as synthetic intermediates, Part V. Part 111: [l]. Part IV: [2]. Part of the planned Ph.D. thesis of F. G., University of Lausanne.