6533b837fe1ef96bd12a1f5c
RESEARCH PRODUCT
Synthesis and biological evaluation of new bicyclic fluorinated uracils through ring-closing metathesis.
Santos FusteroJuan F. Sanz-cerveraSilvia CatalanJose Luis AcenaJulio PieraBegona Fernandezsubject
Bicyclic moleculeNitrileMolecular StructureChemistryOrganic ChemistryGeneral MedicineFluorineRing (chemistry)MetathesisChemical synthesisCombinatorial chemistrychemistry.chemical_compoundRing-closing metathesisSalt metathesis reactionOrganic chemistryRing-opening metathesis polymerisationMoietyUracilAcyclic diene metathesisdescription
Two families of bicyclic fluorinated uracils have been prepared starting from a gem-difluorinated unsaturated nitrile, by means of a ring-closing metathesis reaction to form the new ring, which is fused at the C-5/C-6 or N-1/C-6 positions of the uracil moiety. The selective formation of olefin regioisomers in the metathesis process can be controlled according to the reaction conditions (catalyst, solvent, and temperature). The acaricidal activities of the resulting compounds have also been investigated.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2006-10-03 | The Journal of organic chemistry |