Total synthesis of the thymidine analogue of sinefungin

Article abstract of DOI:10.1080/15257779508009744

The carbon skeleton of 'Sinethymidin' 4 was constructed by two radical coupling reaction. The first step was a coupling of the radical derived from 2 and the unsaturated amide 5. The olefin 6 thus obtained was added to the radical derived from the known N

Full text of DOI:10.1080/15257779508009744

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Nucleosides and Nucleotides
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Total Synthesis of the Thymidine
Analogue of Sinefungin
Derek H. R. Barton b , Stephan D. Gero a , Guillerm Negron c ,
Béatrice Quiclet-Sire a , Mohammad Samadi a & Claire Vincent a
a Institut de Chimie des Substances Naturelles, C.N.R.S. , 91198,
Gif-sur-Yvette, Cedex, France
b Department of Chemistry , Texas A&M University , College Station,
Texas, 77843, U.S.A.
c Area de Quimica, Universidad Autonoma Metropolitana-
Azcapotzalco , Av. San Pa No. 180, C.P. 02200, Mexico D.F., Mexico
Published online: 24 Sep 2006.
To cite this article: Derek H. R. Barton , Stephan D. Gero , Guillerm Negron , Béatrice Quiclet-Sire ,
Mohammad Samadi & Claire Vincent (1995) Total Synthesis of the Thymidine Analogue of Sinefungin,
Nucleosides and Nucleotides, 14:8, 1619-1630, DOI: 10.1080/15257779508009744
To link to this article: http://dx.doi.org/10.1080/15257779508009744
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