In the search for more effective antiviralagentsnucleosides and nucleosideanalogues have been explored extensively. We report the synthesis of a number of acyclicanalogues of guanosine, adenosine, and uridine fluorinated at different sites of the acyclic moiety. All compounds have been obtained in optically pure form by condensing chloromethyl 1,3-disubstituted-2-propyl ethers, chloromethyl 1,3-disubstituted-2-butyl ethers, and 1-chloroethyl 1,3-disubstituted-2-propyl ethers with the desired bases. Open chain fluoroalcohols, needed as starting materials, have been made available by elaborating homochiral fluorinated β-ketosulphoxides. Difluorinated molecules were obtained by DAST treatment of sulphoxide intermediates. In the nucleosideanalogues one or two fluorine atoms are present at the positions corresponding to the 3′ and 5′ carbon atoms of the sugar molecule.

Synthesis of fluorinated analogues of acyclic nucleosides as potential antiviral agents

BRAVO, PIERFRANCESCO;RESNATI, GIUSEPPE;
1989-01-01

Abstract

In the search for more effective antiviralagentsnucleosides and nucleosideanalogues have been explored extensively. We report the synthesis of a number of acyclicanalogues of guanosine, adenosine, and uridine fluorinated at different sites of the acyclic moiety. All compounds have been obtained in optically pure form by condensing chloromethyl 1,3-disubstituted-2-propyl ethers, chloromethyl 1,3-disubstituted-2-butyl ethers, and 1-chloroethyl 1,3-disubstituted-2-propyl ethers with the desired bases. Open chain fluoroalcohols, needed as starting materials, have been made available by elaborating homochiral fluorinated β-ketosulphoxides. Difluorinated molecules were obtained by DAST treatment of sulphoxide intermediates. In the nucleosideanalogues one or two fluorine atoms are present at the positions corresponding to the 3′ and 5′ carbon atoms of the sugar molecule.
1989
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/656747
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