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Acyclic Analogues of Purine Nucleosides with Dimethylaminoethyl and Dimethylaminoethoxyalkyl Side Chains: Preparation, One-and Two-Dimensional 1 H and 13 C NMR Studies.-A new series of purine acyclonucleosides (V), (VI), and (VIII) are prepared by the reaction of protected adenines (I) and (VII) with chloride (IV). They are characterized by NMR spectroscopy. -(PONGRACIC, M.; RAIC, S.; VIKIC-TOPIC, D.; MINTAS, M.; Croat.

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