Stereospecific synthesis and biological evaluations of beta-L-pentofuranonucleoside derivatives of 5-fluorouracil and 5-fluorocytosine

Citation
Jf. Griffon et al., Stereospecific synthesis and biological evaluations of beta-L-pentofuranonucleoside derivatives of 5-fluorouracil and 5-fluorocytosine, EUR J MED C, 36(5), 2001, pp. 447-460
Citations number
39
Categorie Soggetti
Chemistry & Analysis
Journal title
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
ISSN journal
02235234 → ACNP
Volume
36
Issue
5
Year of publication
2001
Pages
447 - 460
Database
ISI
SICI code
0223-5234(200105)36:5<447:SSABEO>2.0.ZU;2-A
Abstract
In the search for new chemotherapeutic agents, we have focused our work on the synthesis and the study of several unnatural beta -L-nucleoside analogu es. In this paper, we report on the synthesis Of beta -L-pentofuranonucleos ides (and their 2 ' -deoxy derivatives) of 5-fluorouracil and their inhibit ory effects on the proliferation of several murine and human tumor cells. T he corresponding 5-fluorocytosine derivatives were also synthesized and the ir anti-HIV and anti-HBV activities have been evaluated. (C) 2001 Editions scientifiques et medicales Elsevier SAS.