Sulfur glycosylation reactions involving 3-allyl-2-thiohydantoin nucleoside bases as potential antiviral and antitumor agents

Article abstract of DOI:10.1080/10426509808029674

3-Allyl-5-(Z)-arylidene-2-thiohydantoins 8a-f were synthesized from the direct condensation of the aromatic aldehydes 7a-f with 3-allyl-2-thiohydantoin (6), which in turn was prepared from the reaction of glycine and allyl isothiocyanate. The alkylation o

Full text of DOI:10.1080/10426509808029674

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Phosphorus, Sulfur, and Silicon
and the Related Elements
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SULFUR GLYCOSYLATION
REACTIONS INVOLVING 3-
ALLYL-2-THIOHYDANTOIN
NUCLEOSIDE BASES AS
POTENTIAL ANTIVIRAL AND
ANTITUMOR AGENTS
Ahmed I. Khodair a c & Jean-Pierre Gesson b
a Chemistry Department, Faculty of Education,
Tanta University (Kafr El-Sheikh Branch), Tanta,
Egypt
b Laboratoire de Chimie XII, Université de Poitiers et
CNRS, 40 Avenue du Recteur Pineau, 86022, Poitiers,
France
c Laboratoire de Chimie XII, Université de Poitiers et
CNRS, 40 Avenue du Recteur Pineau, 86022, Poitiers,
France Fax: E-mail:
Published online: 24 Sep 2006.
To cite this article: Ahmed I. Khodair & Jean-Pierre Gesson (1998): SULFUR
GLYCOSYLATION REACTIONS INVOLVING 3-ALLYL-2-THIOHYDANTOIN NUCLEOSIDE BASES
AS POTENTIAL ANTIVIRAL AND ANTITUMOR AGENTS, Phosphorus, Sulfur, and Silicon
and the Related Elements, 142:1, 167-190
To link to this article: http://dx.doi.org/10.1080/10426509808029674
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