A facile and improved synthesis of tubercidin and certain related pyrrolo[2,3‐d]pyrimidine nucleosides by the stereospecific sodium salt glycosylation procedure

Journal of Heterocyclic Chemistry

Volumn 25, Issue 6, 1988, Pages 1893-1898

  Ramasamy, Kandasamy ^a   Imamura, Nobutaka ^a   Robins, Roland K ^a   Revankar, Ganapathi R ^a  

^a Nucleic Acid Research Institute ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

7 DEAZAGUANOSINE; DEOXY 7 DEAZAGUANOSINE; PYRROLO[2,3 D]PYRIMIDINE NUCLEOSIDE; TUBERCIDIN; UNCLASSIFIED DRUG;

DRUG STRUCTURE; DRUG SYNTHESIS; NONHUMAN; NUCLEAR MAGNETIC RESONANCE;

EID: 0024206813     PISSN: 0022152X     EISSN: 19435193     Source Type: Journal    
DOI: 10.1002/jhet.5570250652     Document Type: Article

References (50)

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2. Synthese von 2-Amino-3, 7-(β-D-ribofuranosyl)-4H-pyrrolo[2,3-d] pyrimidin-4-on - 7-Desazaguanosin - der Stammverbindung des Nucleosids Q
3. Direct synthesis of pyrrole nucleosides by the stereospecific sodium salt glycosylation procedure
4. α-Thymidin
5. Recherehes sur les nucleosides de synthese. III. Sur un nouveau critere de determination de la configuration anomere des nucleosides ribosidiques
6. 2-Deoxy-D-erythro-pentose. IX.1Some Relationships among the Rotations of Acylated Aldopentoses, Aldopentosyl Halides, and Anhydropentitols