Abstract
AbstractThe key intermediates allyloxyquinoxaline 2a–c and N‐allylquinoxaline 3a–c were used to synthesize a number of acyclonucleosides whose chemical modifications include quinoxaline ring and the acyclic part is either N1‐propanediol or 3‐hydroxy‐ propyl substituents and their O‐analogues. These compounds were characterized by elemental analysis, MALDI MS, and NMR data. © 2006 Wiley Periodicals, Inc. Heteroatom Chem 17:280–288, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20203
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