Synthesis and anti-HIV activity of carbocyclic ring-enlarged 4′,1′a-methano oxetanocin analogues

Article abstract of DOI:10.1080/07328319708006132

Synthesis of carbocyclic ring-enlarged 4′,1′a-methano oxetanocin analogues via completely regioselective opening of cyclic sulfites by sodium azide or purine bases is described. Copyright

Full text of DOI:10.1080/07328319708006132

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Synthesis and Anti-HIV Activity of
Carbocyclic Ring-Enlarged 4′,1′a-
Methano Oxetanocin Analogues
Lak S. Jeong a , Min Bae b , Moon W. Chun b & Victor E. Marquez
c
a Laboratory of Medicinal Chemistry , College of Pharmacy, Ewha
Womans University , Seoul, 120-750, Korea
b College of Pharmacy, Seoul National University , Seoul,
151-742, Korea
c Laboratory of Medicinal Chemistry, Division of Basic Sciences ,
National Cancer Institute, NIH , Bethesda, MD, 20892, USA
Published online: 16 Aug 2006.
To cite this article: Lak S. Jeong , Min Bae , Moon W. Chun & Victor E. Marquez (1997) Synthesis
and Anti-HIV Activity of Carbocyclic Ring-Enlarged 4′,1′a-Methano Oxetanocin Analogues,
Nucleosides and Nucleotides, 16:7-9, 1059-1062, DOI: 10.1080/07328319708006132
To link to this article: http://dx.doi.org/10.1080/07328319708006132
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