Carbocyclic analogues of 3',4'-didehydro-2'-deoxyribofuranosyl-2,4(1H,3H)- pyrimidinediones

Article abstract of DOI:10.1080/15257779408010673

A new method for obtaining carbocyclic analogues of 3',4'-didehydro- 2,4(1H,3H)-pyrimidinedione nucleosides in good yields consists of the reaction of the carbocyclic 2,3'-anhydronucleosides with lithium chloride in dimethylformamide. Small amounts of the

Full text of DOI:10.1080/15257779408010673

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Nucleosides and Nucleotides
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Carbocyclic Analogues
of 3′,4′-Didehydro-2′-
deoxyribofuranosyl-2,4(1H,3H)-
pyrimidinediones
C. Allen O'Dell a & Y. Fulmer Shealy a
a Organic Chemistry Research Department , Southern Research
Institute , 2000 Ninth Avenue South, Birmingham, Alabama, 35255,
U.S.A.
Published online: 24 Sep 2006.
To cite this article: C. Allen O'Dell & Y. Fulmer Shealy (1994) Carbocyclic Analogues of 3′,4′-
Didehydro-2′-deoxyribofuranosyl-2,4(1H,3H)-pyrimidinediones, Nucleosides and Nucleotides, 13:9,
1929-1937, DOI: 10.1080/15257779408010673
To link to this article: http://dx.doi.org/10.1080/15257779408010673
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