Coupling of 2,6-dichloropurine and 2,6-dichlorodeazapurines with ribose and ribose modified sugars

Citation
S. Vittori et al., Coupling of 2,6-dichloropurine and 2,6-dichlorodeazapurines with ribose and ribose modified sugars, NUCLEOS NUC, 18(4-5), 1999, pp. 587-590
Citations number
12
Categorie Soggetti
Biochemistry & Biophysics
Journal title
NUCLEOSIDES & NUCLEOTIDES
ISSN journal
07328311 → ACNP
Volume
18
Issue
4-5
Year of publication
1999
Pages
587 - 590
Database
ISI
SICI code
0732-8311(1999)18:4-5<587:CO2A2W>2.0.ZU;2-6
Abstract
Substituted purine and deazapurine nucleosides are of great interest in med icinal chemistry. Furthermore, 3'-deoxynucleosides exhibit a number of biol ogical activities. In this research the coupling of 2,6-dichloro-1- or 3-de azapurine with protected 3'-deoxyribose is reported. Depending upon couplin g conditions and base structure, different anomeric and isomeric mixtures h ave been obtained. Extensive studies, utilizing chemical and physical metho ds, have been performed to assign the correct configuration to the resultin g nucleosides.