Volume 22, Issue 15
Natural Products
Full Access

ChemInform Abstract: Nucleosides. Part 153. Synthesis of 1-Methyl-5-(3-azido-2,3-dideoxy-. beta.-D-erythro-pentofuranosyl)uracil and 1-Methyl-5-(3-azido-2,3- dideoxy-2-fluoro-β-D-arabinofuranosyl)uracil. The C-Nucleoside Isostere of 3′-Azido-3′-deoxythymidine and Its 2′-“Up”-Fluoro Analogue.

E. SOCHACKA

E. SOCHACKA

Sloan-Kettering Inst. Cancer Res., Memorial Sloan-Kettering Cancer Center, Sloan-Kettering Div. Grad. School Med. Sci., Cornell Univ., New York, NY 10021, USA

Search for more papers by this author
B. NOWROT

B. NOWROT

Sloan-Kettering Inst. Cancer Res., Memorial Sloan-Kettering Cancer Center, Sloan-Kettering Div. Grad. School Med. Sci., Cornell Univ., New York, NY 10021, USA

Search for more papers by this author
K. W. PANKIEWICZ

K. W. PANKIEWICZ

Sloan-Kettering Inst. Cancer Res., Memorial Sloan-Kettering Cancer Center, Sloan-Kettering Div. Grad. School Med. Sci., Cornell Univ., New York, NY 10021, USA

Search for more papers by this author
K. A. WATANABE

K. A. WATANABE

Sloan-Kettering Inst. Cancer Res., Memorial Sloan-Kettering Cancer Center, Sloan-Kettering Div. Grad. School Med. Sci., Cornell Univ., New York, NY 10021, USA

Search for more papers by this author
First published: April 16, 1991

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

The compounds (VIII) mentioned in the title are synthesized as outlined in the reaction scheme. Other attempts to get these compounds using different synthetic routes are also described. (VIIIa) is a C- nucleoside isostere of the potent anti-AIDS nucleoside AZT. However, neither (VIIIa) nor (VIIIb) show any significant inhibitory activity against HIV in H9 cells.

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.