Efficient stereoselective synthesis of new C-nucleosides via intramolecular Mitsunobu cyclization

Article abstract of DOI:10.1080/15257779908041510

We have studied the stereoselective synthesis of new C-nucleosides by heteroarylation of the protected γ-ribonolactone by means of heteroaromatic systems such as indole, thiazoles, imidazoles and benzimidazoles. We have observed that the first anion addit

Full text of DOI:10.1080/15257779908041510

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Nucleosides and Nucleotides
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Efficient Stereoselective Synthesis of
New C-Nucleosides via Intramolecular
Mitsunobu Cyclization
R. Benhida a b , D. Guianvarch a b , J-L. Fourrey a b & J. S. Sun a b
a Institut de Chimie des Substances Naturelles - CNRS , 91198, Gif
sur Yvette
b Laboratoire de Biophysique , Muséum Nationale d'Histoires
Naturelles , 23 rue Cuvier, 75005, Paris
Published online: 04 Oct 2006.
To cite this article: R. Benhida , D. Guianvarch , J-L. Fourrey & J. S. Sun (1999) Efficient
Stereoselective Synthesis of New C-Nucleosides via Intramolecular Mitsunobu Cyclization, Nucleosides
and Nucleotides, 18:4-5, 603-604, DOI: 10.1080/15257779908041510
To link to this article: http://dx.doi.org/10.1080/15257779908041510
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