The synthesis of carbocyclic 5'-nor thymidine and an isomer as oligonucleotide monomers

Article abstract of DOI:10.1080/07328319908044851

The chiral synthesis of (1S,3S,4S)-1-(3,4-dihydroxycyclopent-1-yl)-1H- thymine (carbocyclic 5,-nor thymidine, 4) has been achieved in 5 steps from (+)-(1R,4S)-4-hydroxy-2-cyclopenten-1-yl acetate (5) and N³-benzoylthymine. Compound 4 is viewed

Full text of DOI:10.1080/07328319908044851

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Nucleosides and Nucleotides
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The Synthesis of Carbocyclic 5′-
Nor Thymidine and an Isomer as
Oligonucleotide Monomers
Vishnumurthy R. Hegde a , Katherine L. Seley a , Xing Chen a
Stewart W. Schneller a
&
a Department of Chemistry, Auburn University, Auburn, AL,
36849-5312
Published online: 04 Oct 2006.
To cite this article: Vishnumurthy R. Hegde , Katherine L. Seley , Xing Chen & Stewart W. Schneller
(1999) The Synthesis of Carbocyclic 5′-Nor Thymidine and an Isomer as Oligonucleotide Monomers,
Nucleosides and Nucleotides, 18:8, 1905-1910
To link to this article: http://dx.doi.org/10.1080/07328319908044851
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