A SYNTHETIC STRATEGY TO A NEW CLASS OF CYCLOALKANE RING-FUSED PYRIDINE NUCLEOSIDES AS POTENTIAL ANTI-HIV AGENTS

Citation
Geh. Elgemeie et al., A SYNTHETIC STRATEGY TO A NEW CLASS OF CYCLOALKANE RING-FUSED PYRIDINE NUCLEOSIDES AS POTENTIAL ANTI-HIV AGENTS, Nucleosides & nucleotides, 17(5), 1998, pp. 855-868
Citations number
11
Categorie Soggetti
Biology
Journal title
ISSN journal
07328311
Volume
17
Issue
5
Year of publication
1998
Pages
855 - 868
Database
ISI
SICI code
0732-8311(1998)17:5<855:ASSTAN>2.0.ZU;2-J
Abstract
Condensation of cyanothioacetamide or cyanoacetamide with sodium salts of 2-formyl-1-cycloalkanones afforded the corresponding cycloalkane r ing fused pyridine-2(1H)-thiones and -2-pyridones. The latter compound s served as a key intermediates for the synthesis of a new class of cy cloalkane ring fused pyridine glycosides.