Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5280258 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
Carbocyclic nucleosides substituted at the C-6â² position are receiving increasing attention. Chiral synthetic accessibility to the biologically promising 6â²-β-fluoroaristeromycin is lacking. Its preparation and that of the 5â²-nor analogue are described. Along the way, a new method to aristeromycin arose as an outgrowth of a requisite structure proof.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Xue-qiang Yin, Stewart W. Schneller,