Journal of Heterocyclic Chemistry · 2000 · 38 citations · 13 references
PharmacyChemistryMedicinal ChemistryDrug DesignDrug DiscoveryOrganic ChemistryCoordination ChemistryHeterocycle SynthesisHeterocyclic ChemistryLead Compound DesignLigand BindingLigand-based DesignChemical Synthesis Of AnaloguesHeterocyclic Medicinal ChemistryMedicinal HeterocyclesPyrazine Chemistry
Abstract The synthesis is described of a set of new N ‐heterocyclic compounds which are derivatives of 1,10‐phenanthroline. The compounds are designed to be general purpose chelating agents which could function as tri‐, tetra‐ or hexadentate ligands with transition metal ions. Fused‐ring molecular components have been included in the design of the compounds so that they may function as binding agents to DNA through intercalation. This includes the synthesis of substituted derivatives of pyrazino[2,3‐ f ][1,10]phenanthroline and dipyrido[3,2‐ a :2′3′‐ c ]phenazine.
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A molecular light switch for DNA: Ru(bpy)2(dppz)2+
Alan E. Friedman, J.‐C. Chambron, Jean Pierre Sauvage et al. · Journal of the American Chemical Society · 1990 · 1.4K citations