Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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A New Method for the Synthesis of Some Pyridazine Nucleosides

  • Yoon, Yong-Jin (Department of Chemistry, College of Natural Sciences, Gyongsang National University) ;
  • Wise, Dean S. (Department of Medicinal Chemistry, College of Pharmacy, The University of Michigon) ;
  • Townsend, L. B. (Department of Medicinal Chemistry, College of Pharmacy, The University of Michigan)
  • Published : 1987.06.20
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Abstract

Some pyridazin-6-one nucleosides have been prepared directly without silylation of heterocyclic base using iodine catalyst, a new type Friedel-Crafts catalyst.

Keywords

References

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  1. ChemInform Abstract: A New Method for the Synthesis of Some Pyridazine Nucleosides. vol.18, pp.52, 1987, https://doi.org/10.1002/chin.198752357
  2. Pyridazines with heteroatom substituents in position 3 and 5, part 1: 5-Hydroxy-3(2H)-pyridazinone and its derivatives vol.120, pp.4, 1987, https://doi.org/10.1007/bf00811746
  3. Iodine-promoted ribosylation leads to a facile acetonide-forming reaction vol.344, pp.16, 2009, https://doi.org/10.1016/j.carres.2009.08.026
  4. Iodine Monochloride Facilitated Deglycosylation, Anomerization, and Isomerization of 3-Substituted Thymidine Analogues vol.33, pp.12, 1987, https://doi.org/10.1080/15257770.2014.945648