Synthesis of sugar-modified 2,6-diaminopurine and guanine nucleosides from guanosine via transformations of 2-aminoadenosine and enzymatic deamination with adenosine deaminase Article

Robins, MJ, Zou, RM, Hansske, F et al. (1997). Synthesis of sugar-modified 2,6-diaminopurine and guanine nucleosides from guanosine via transformations of 2-aminoadenosine and enzymatic deamination with adenosine deaminase . CANADIAN JOURNAL OF CHEMISTRY, 75(6), 762-767. 10.1139/v97-092

Open Access International Collaboration

cited authors

  • Robins, MJ; Zou, RM; Hansske, F; Wnuk, SF

sustainable development goals

authors

publication date

  • June 1, 1997

published in

keywords

  • 2',3'-DIDEOXYNUCLEOSIDES
  • 2,6-diaminopurine nucleosides
  • ACID RELATED-COMPOUNDS
  • ANALOGS
  • BIOLOGICAL EVALUATION
  • Chemistry
  • Chemistry, Multidisciplinary
  • HIV REPLICATION
  • HUMAN IMMUNODEFICIENCY VIRUS
  • PURINE
  • Physical Sciences
  • RIBONUCLEOSIDES
  • STEREOSELECTIVE CONVERSION
  • SYSTEMATIC SYNTHESIS
  • Science & Technology
  • adenosine deaminase
  • deoxygenation
  • guanine nucleosides
  • nucleosides

Digital Object Identifier (DOI)

publisher

  • NATL RESEARCH COUNCIL CANADA

start page

  • 762

end page

  • 767

volume

  • 75

issue

  • 6