Carbocyclic Sinefungin.

Tetrahedron Lett

Department of Chemistry and Biochemistry, Auburn University Auburn, Alabama 36849-5312.

Published: July 2007

(3aS,4S,6R,6aR)-Tetrahydro-2,2-dimethyl-6-vinyl-3aH-cyclopenta[d][1,3]-dioxol-4-ol, itself available from ribose, provided a convenient entry point for an 18-step preparation of carbocyclic sinefungin. This procedure is adaptable to a number of carbocyclic sinefungin analogs with diversity of heterocyclic base and in the amino acid bearing side chain.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2031829PMC
http://dx.doi.org/10.1016/j.tetlet.2007.05.079DOI Listing

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