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
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.