SYNTHESIS OF 4 STEREOISOMERS OF CARBOCYCLIC 5'-NOR D4A AND EVALUATIONOF THEIR TRIPHOSPHATES AS SUBSTRATES FOR DNA-POLYMERASES

Citation
N. Dyatkina et al., SYNTHESIS OF 4 STEREOISOMERS OF CARBOCYCLIC 5'-NOR D4A AND EVALUATIONOF THEIR TRIPHOSPHATES AS SUBSTRATES FOR DNA-POLYMERASES, Nucleosides & nucleotides, 14(3-5), 1995, pp. 723-726
Citations number
10
Categorie Soggetti
Biology
Journal title
ISSN journal
07328311
Volume
14
Issue
3-5
Year of publication
1995
Pages
723 - 726
Database
ISI
SICI code
0732-8311(1995)14:3-5<723:SO4SOC>2.0.ZU;2-9
Abstract
A method was developed for synthesis of the four stereoisomeric enanti omerically pure 5'-nor carbocyclic nucleosides 4b, ent-4b, 10 and ent- 10 starting from the common enantiomerically pure allylic monoacetate 1. Nucleoside analogues were converted to the corresponding triphospha te derivatives 6, ent-6, 12, and ent-12. The substrate properties of t he latters towards different DNA polymerases were evaluated.