A synthetic approach to carbocyclic sinefungin

Article abstract of DOI:10.1080/07328319808004308

An approach to an asymmetric synthesis of carbocyclic sinefungin (cSF) 2 is proposed. The sequence, which uses an original radical based chemistry for C-C bond formation, led to the immediate precursor 18 of the protected desired compound. While the overall yield is modest, it is noticeable that only a limited number of steps are needed to obtain the target compound.

Full text of DOI:10.1080/07328319808004308

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Nucleosides and Nucleotides
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A Synthetic Approach to Carbocyclic
Sinefungin
Adilson D. Da Silva a , Edmilson JoseMaria a , Pierre Blanchard b ,
Jean-Louis Fourrey b & Malka Robert-Gero b
a Laboratorio de Ciencias Químicas , CCT, UENF , Campos dos
Goytacazes, RJ, 28015 620, Brasil
b Institut de Chimie des Substances Naturelles, CNRS , Gif-sur-
Yvette, 91198, France
Published online: 16 Aug 2006.
To cite this article: Adilson D. Da Silva , Edmilson JoseMaria , Pierre Blanchard , Jean-Louis Fourrey
& Malka Robert-Gero (1998) A Synthetic Approach to Carbocyclic Sinefungin, Nucleosides and
Nucleotides, 17:12, 2175-2187, DOI: 10.1080/07328319808004308
To link to this article: http://dx.doi.org/10.1080/07328319808004308
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