Kundu, NG
Das, P.
Balzarini, Jan
[KUL]
De Clercq, Etienne
[UCL]
[E]-6-(2-Acylvinyl)uracils and their corresponding 1-(2-hydroxyethoxy)methyl derivatives were synthesized through palladium-catalyzed reactions which involved an interesting rearrangement. Some of the acylvinyl uracils (3, 4, and 5) and the acyclonucleosides (8 and 10) showed pronounced activity against human T-lymphocyte Molt 4/C8 and CEM cells. However, they were less toxic to murine L1210 and FM3A cells. The compounds did not have any marked antiviral activity. (C) 1997 Elsevier Science Ltd.
Bibliographic reference |
Kundu, NG ; Das, P. ; Balzarini, Jan ; De Clercq, Etienne. Uracil derivatives and analogues .24. Palladium-catalyzed synthesis of [E]-6-(2-acylvinyl)uracils and [E]-6-(2-acylvinyl)-1-[(2-hydroxyethoxy)methyl]uracils - their antiviral and cytotoxic activities. In: Bioorganic & Medicinal Chemistry : the tetrahedron journal for research at the interface of chemistry and biology, Vol. 5, no. 11, p. 2011-2018 (1997) |
Permanent URL |
http://hdl.handle.net/2078.1/45844 |