132813-67-3Relevant articles and documents
Enantiospecific Synthesis of 3'-Hetero-dideoxy Nucleoside Analogues as Potential Anti-HIV Agents
Jones, Martin F.,Noble, Stewart A.,Robertson, Colin A.,Storer, Richard,Highcock, Rona M.,Lamont, R. Brian
, p. 1427 - 1436 (2007/10/02)
Two series of analogues of 2',3'-dideoxy carbocyclic nucleosides, in which the 3'-carbon atom is replaced by either an oxygen or a sulfur atom, have been prepared enantiospecifically from diacetone-L-glucose and diacetone-D-glucose respectively.Within eac
TETRAHYDROTHIOPHENE NUCLEOSIDES AS POTENTIAL ANTI-HIV AGENTS
Jones, Martin F.,Noble, Stewart A.,Robertson, Colin A.,Storer, Richard
, p. 247 - 250 (2007/10/02)
A series of novel tetrahydrothiophene nucleosides have been prepared in homochiral form from D-glucose and assessed as anti-HIV agents in whole cell assay.