Synthesis of 1-deazaadenosine analogues of (2′→5′) ApApA

Article abstract of DOI:10.1080/07328319608002397

Synthesis of (2′→5′)ApApA analogues containing 1-deazaadenosine at different positions is described (32-34). The approach used the phosphotriester methodology in solution and utilized 3′-O-benzoylated derivatives of the N⁶-protected 5′-O-monome

Full text of DOI:10.1080/07328319608002397

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Nucleosides and Nucleotides
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Synthesis of 1-Deazaadenosine
Analogues of (2′→5′) ApApA
Igor A. Mikhailopoulo a , Elena N. Kalinichenko a , Tatjana L.
Podkopaeva a , Thomas Wenzel b , Helmut Rosemeyer b & Frank
L. Seela b
a Institute of Bioorganic Chemistry, Byelorussian Academy of
Sciences , 220141, Minsk, Byelorussia
b Laboratorium für Organische und Bioorganische Chemie,
Institut für Chemie, Universiat Osnabrück , D-49076, Osnabrück,
Germany
Published online: 21 Aug 2006.
To cite this article: Igor A. Mikhailopoulo , Elena N. Kalinichenko , Tatjana L. Podkopaeva ,
Thomas Wenzel , Helmut Rosemeyer & Frank L. Seela (1996) Synthesis of 1-Deazaadenosine
Analogues of (2′→5′) ApApA, Nucleosides and Nucleotides, 15:1-3, 445-464
To link to this article: http://dx.doi.org/10.1080/07328319608002397
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