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In this letter, we successfully explored a cascade Pd/Cu-catalyzed intermolecular C(sp3)–H arylation of amides and intramolecular C–N coupling reaction. This method provides a one-pot strategy to synthesize 3,4-2H-quinolinone with good regioselectivity of C–H arylation and C–N coupling from C–I and C–X bonds from readily available starting materials.

The first phthalocyanine (Pc) macrocycle-containing [FeFe]-hydrogenase model complex, (i-BuO)8PcRu(CO)(μ-PDT)[(Ph2P)2NCH2C5H4N]Fe2(CO)4 (6), has been prepared by a multistep synthetic route. The treatment of 4-picolylamine with Ph2PCl/Et3N in CH2Cl2 at room temperature gave 4-picolyl-substituted azadiphosphine (Ph2P)2NCH2C5H4N (1), whereas further treatment of 1 with diiron complex (μ-PDT)Fe2(CO)6 in refluxing o-xylene produced the 4-picolylazadiphosphine-chelated diiron complex (μ-PDT)[(Ph2P)2NCH2C5H4N]Fe2(CO)4 (2). While 3,6-dihydroxyphthalonitrile reacted with i-BuBr/K2CO3 in DMF at 80 °C to give 3,6-diisobutoxyphthalonitrile 3, further reaction of 3 with lithium wire in refluxing i-BuOH afforded isobutoxyphthalocyanine (i-BuO)8PcH2 (4). Furthermore, 4 reacted with Ru3(CO)12 in refluxing PhCN to give ruthenium phthalocyanine (i-BuO)8PcRu(CO)2 (5). Finally, CO substitution reaction of 5 with diiron complex 2 in the presence of Me3NO in CH2Cl2 resulted in formation of the targeted model complex 6. While ...

Selective cleavage of an inert C-C bond followed by C-O/N bond formation through a long-distance aryl migration from a carbon to a nitrogen center via Ag catalysis is reported. The migration products were easily converted into γ-hydroxy amines and tetrahydroquinoline derivatives in quantitative yields. Preliminary mechanistic studies indicated a radical pathway.

Two new ferrocenyl (Fc) group containing 1,5-diaza-3,7-diphosphacyclooctane ligands, PFc2NAr2 (1, Ar = Ph; 2, Ar = p-BrC6H4), were prepared by reaction of FcPH2 with 2 equiv of paraformaldehyde in glycol followed by treatment of the resulting FcP(CH2OH)2 with 1 equiv of aniline or p-bromoaniline in 79% and 67% yields, respectively; however, ligands 1 and 2 could be also prepared by treatment of the isolated and purified FcP(CH2OH)2 with 1 equiv of aniline or p-bromoaniline under similar conditions in 80% and 72% yields, respectively. Further treatment of 1 or 2 with the complex salt [Ni(MeCN)6](BF4)2 in MeCN at room temperature resulted in formation of the first ferrocenyl-containing complexes [Ni(PFc2NAr2)2](BF4)2 (3, Ar = Ph; 4, Ar = p-BrC6H4) in 95% and 90% yields, respectively. Compounds 1–4 were structurally characterized by elemental analysis and spectroscopy and particularly for 1, 2, and 4 by X-ray crystallography. When the cyclic voltammetric behavior of 1–4 was investigated, 3 and 4 were found t...