Stereoselective synthesis of carbocyclic α-L-homonucleosides

Article abstract of DOI:10.1080/15257779908041509

The synthesis of several optically pure carbocyclic α-L-isomeric homonucleosides [3a-e, 6a,b, 7a,b, 10a-d] is reported. The (1R,5S)-2- oxabicyclo[3.3.0]oct-6-en-3-one 1 was used as a chiral starting material.

Full text of DOI:10.1080/15257779908041509

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Nucleosides and Nucleotides
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Stereoselective Synthesis of Carbocyclic
α-L-Homonucleosides
L. A. Agrofoglio a , F. Girard a , C. Demaison a , M-G. Lee a , P.
Roingeard b & A. Fridland c
a I. C. O. A., associé au CNRS , 45100, Orléans, France
b Lab. Virol. & Biol. Cell. , EP CNRS 117, CHU Bretonneau, Tours,
France
c Dept. Infectious Diseases , St. Jude Children's Research Hospital ,
Memphis, TN, 38105-2794, USA
Published online: 04 Oct 2006.
To cite this article: L. A. Agrofoglio , F. Girard , C. Demaison , M-G. Lee , P. Roingeard & A. Fridland
(1999) Stereoselective Synthesis of Carbocyclic α-L-Homonucleosides, Nucleosides and Nucleotides,
18:4-5, 601-602, DOI: 10.1080/15257779908041509
To link to this article: http://dx.doi.org/10.1080/15257779908041509
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