Abstract
A Synthetic entry to a novel class of cyclopentyl carbocyclic nucleusides and other functional derivatives, in enantiopure form, is presented. As a structural feature of these compounds, the base-moiety is separated from the carbocyclic ring by a C2-chain containing a quaternary stereogenic center and additional chemical functions.
| Original language | English |
|---|---|
| Pages (from-to) | 3421-3430 |
| Journal | Tetrahedron Asymmetry |
| Volume | 8 |
| Issue number | 20 |
| DOIs | |
| Publication status | Published - 23 Oct 1997 |
Fingerprint Dive into the research topics of 'A synthetic approach to a novel class of enantiopure cyclopentyl carbocyclic nucleosides and related compounds'. Together they form a unique fingerprint.
Cite this
Díaz, M., & Ortuño, R. M. (1997). A synthetic approach to a novel class of enantiopure cyclopentyl carbocyclic nucleosides and related compounds. Tetrahedron Asymmetry, 8(20), 3421-3430. https://doi.org/10.1016/S0957-4166(97)00401-1