An improved method for the preparation of 2′,3′-unsaturated nucleosides: Synthesis of stereospecifically labelled ketonucleosides

Carbohydrate Research

Volumn 176, Issue 2, 1988, Pages 219-229

  Herscovici, Jean ^a   Montserret, Roland ^a   Antonakis, Kostas ^a  

^a Institut de Recherches Scientifiques sur le Cancer   (France)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0342681504     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/0008-6215(88)80133-2     Document Type: Article

References (32)

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2. 1038. Unsaturated carbohydrates. Part II. Three reactions leading to unsaturated glycopyranosides
3. Unsaturated carbohydrates. Part IX. Synthesis of 2,3-dideoxy-?-D-erythro-hex-2-enopyranosides from tri-O-acetyl-D-glucal
4. Use of Unsaturated Sugars as Alkylating Agents. Addition of Enol Esters and Ethers to Glycals
5. C-glycopyranosides from the reaction of acetylated glycals with ?-diketones
6. Unsaturated carbohydrates. Part XIV. The isomerisation of hex-2-enopyranosylpurine nucleoside derivatives
7. A facile synthesis of .ALPHA.-C-ribofuranosides from 1-O-acetyl ribose in the presence of trityl perchlolate.
8. A facile synthesis of .ALPHA.-glucosides and .ALPHA.-ribosides from the corresponding 1-O-acyl sugars and alcohols in the presence of trityl perchlorate.
9. New oxidative systems for alcohols: molecular sieves with chromium(VI) reagents
10. Verzweigte Zucker, XXIII: 1,4-Addition an Hex-1-enopyran-3-ulosen zu Oct-2-ulosonsäuren