Radical mediated synthesis of 3'-α-C-allenyl-2',3'-dideoxythymidine as a non-polar analogue of AZT

Article abstract of DOI:10.1080/15257779508012368

The synthesis of the novel modified nucleoside (1) exhibiting the 1,2- propadienyl [allenyl] group at the 3'-α-position is described. The 3'-C-C bond was formed by radical reaction between triphenylprop 2-ynylstannane (2) and the 3'-bromo(iodo)-2',3'-dide

Full text of DOI:10.1080/15257779508012368

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Radical Mediated Synthesis of 3′-α-C-
Allenyl-2′,3′-dideoxythymidine as a Non-
polar Analogue of AZT
S. Becouarn a , S. Czernecki a & J. M. Valéry a
a Université Pierre et Marie Curie, Laboratoire de Chimie des
Glucides , 4 Place Jussieu, 75005, Paris, France
Published online: 16 Feb 2007.
To cite this article: S. Becouarn , S. Czernecki & J. M. Valéry (1995) Radical Mediated Synthesis of
3′-α-C-Allenyl-2′,3′-dideoxythymidine as a Non-polar Analogue of AZT, Nucleosides and Nucleotides,
14:3-5, 307-309
To link to this article: http://dx.doi.org/10.1080/15257779508012368
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