Synthesis of N-glycosylated pyridines as new antimetabolite agents

Article abstract of DOI:10.1080/07328319908044886

Condensation of cyanoacetamide and cyanothioacetamide with the sodium salts of α-(hydroxymethylene)alkanones afforded the pyridine-2(1H)-ones and their corresponding thiones 3. Compounds 3 served as a key intermediates for the synthesis of N-glycosylated pyridines.

Full text of DOI:10.1080/07328319908044886

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Nucleosides and Nucleotides
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Synthesis of N-Glycosylated Pyridiines as
New Antimetabolite Agents
Badria A. Hussain a , Adel M. Attia a & Galal E. H. Elgemeie b
a Chemistry Department, Faculty of Science , Qatar University ,
Doha, Qatar
b Chemistry Department , Faculty of Science, Helwan University ,
Helwan, Cairo, Egypt
Published online: 04 Oct 2006.
To cite this article: Badria A. Hussain , Adel M. Attia & Galal E. H. Elgemeie (1999) Synthesis of
N-Glycosylated Pyridiines as New Antimetabolite Agents, Nucleosides and Nucleotides, 18:10,
2335-2343, DOI: 10.1080/07328319908044886
To link to this article: http://dx.doi.org/10.1080/07328319908044886
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