作者:Katherine L. Seley、Sylvester L. Mosley、Fanxing Zeng
DOI:10.1021/ol035696q
日期:2003.11.1
Isoadenosine (IsoA), a structural isomer of adenosine, was shown to possess interesting biological activity but was inherently unstable. In an effort to overcome this, we have designed a series of carbocyclic IsoA analogues, combining the unique connectivity of IsoA with the structural features of some biologically significant Neplanocin A analogues. Their design, synthesis, and structural elucidation is reported.