Synthesis and biological activity of 5-azacytosine nucleosides derived from 4-thio-2-deoxy-L-threo-pentofuranose and 4-thio-2-deoxy-D-erythro-pentofuranose

Authors
Cappellacci, L Tiwari, KN Montgomery, JA Secrist, JA
Citation
L. Cappellacci et al., Synthesis and biological activity of 5-azacytosine nucleosides derived from 4-thio-2-deoxy-L-threo-pentofuranose and 4-thio-2-deoxy-D-erythro-pentofuranose, NUCLEOS NUC, 18(4-5), 1999, pp. 613-614
Citations number
3
Categorie Soggetti
Biochemistry & Biophysics
Journal title
NUCLEOSIDES & NUCLEOTIDES
ISSN journal
07328311 → ACNP
Volume
18
Issue
4-5
Year of publication
1999
Pages
613 - 614
Database
ISI
SICI code
0732-8311(1999)18:4-5<613:SABAO5>2.0.ZU;2-W
Abstract
1-O-Acetyl-2-deoxy-3,5-di-O-toluoyl-4-thio-D-erythro-pentofuranose and and 2-deoxy-1,3,5-tri-O-acetyl-4-thio-L-threo-pentofuranose were coupled with 5 -azacytosine to obtain alpha and beta anomers of nucleosides.