Synthesis and Biological Evaluation of a Series of Substituted 2-Pyridine C-Nucleosides
Article 1985 en
Authors
MB
Marc Belmans
EE
Eddy L. Esmans
RD
R. Dommisse
Abstract
1 min read
Abstract Condensation of 2-lithio-pyridine and the four isomers of 2-lithio-picoline with 2,4:3,5-di-O-benzylidene-aldehydo-D-ribose, gives the D-allo- and D-altro-isomers of 2-(2,4:3,5-di-O-benzylidenepentitol-l-yl)-pyridine and the corresponding isomers of the four picoline-addition products in a good yields. On treatment with dilute hydrochloric acid or formic acid the corresponding pentitols were obtained. None of these pentitols showed an inhibitory effect on virus replication or tumor cell growth.
Marc Belmans, I. Vrijens, Eddy L. Esmans, R. Dommisse, J. A. Lepoivre, F. C. Alderweireldt, L. B. TOWNSEND, Linda L. Wotring, Jan Balzarini, De Clercq Erik
Marc Belmans, I. Vrijens, Eddy L. Esmans, R. Dommisse, J. A. Lepoivre, F. C. Alderweireldt, L. B. TOWNSEND, Linda L. Wotring, Jan Balzarini, De Clercq Erik
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