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- W4281567180 endingPage "578" @default.
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- W4281567180 abstract "This paper presented the efficiency of different Pd-based catalytic systems in a series of SM reactions of 4,5-dibromo-2-methylpyridazin-3(2H)-one with ferroceneboronic acid, ferrocene-1,1′-diboronoc acid, and its bis-pinacol ester. In addition to the disubstituted product, these transformations afford substantial amounts of isomeric 4- and 5-ferrocenyl-2-methylpyridazin-3(2H)-ones, and a unique asymmetric bi-pyridazinone-bridged ferrocenophane with a screwed molecular architecture. The reactions of phenylboronic acid, conducted under the conditions, are proven to be the most reductive in the conversions of ferroceneboronic acid, and produce 2-methyl-4,5-diphenylpyridazin-3(2H)-one as single product, supporting our view about solvent-mediated hydrodehalogenations that are supposed to proceed via the assistance of the ferrocenyl group present in the reaction mixture, or attached to the bromo-pyridazinone scaffold, which is constructed in the first SM coupling of the heterocyclic precursor. A comparative DFT modelling study on the structures and possible transformations of relevant bromo-, ferrocene- and phenyl-containing carbopalladated intermediate pairs was carried out, providing reasonable mechanisms suitable to account for the apparently surprising regioselectivity of the alternative hydrodebromination processes, and for the formation of the ferrocenophane product. Supporting the results of DFT modelling studies, the implication of DMF as a hydrogen transfer agent in the hydrodebromination reactions is evidenced by deuterium labelling experiments using the solvent mixtures DMF-d7–H2O (4:1) and DMF–D2O (4:1). The organometallic products display antiproliferative effects on human malignant cell lines." @default.
- W4281567180 created "2022-05-27" @default.
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- W4281567180 date "2022-05-24" @default.
- W4281567180 modified "2023-10-18" @default.
- W4281567180 title "Synthetic and DFT Modeling Studies on Suzuki–Miyaura Reactions of 4,5-Dibromo-2-methylpyridazin-3(2H)-one with Ferrocene Boronates, Accompanied by Hydrodebromination and a Novel Bridge-Forming Annulation In Vitro Cytotoxic Activity of the Ferrocenyl–Pyridazinone Products" @default.
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- W4281567180 cites W1969964192 @default.
- W4281567180 cites W1971380639 @default.
- W4281567180 cites W1975755749 @default.
- W4281567180 cites W1976208125 @default.
- W4281567180 cites W1978890358 @default.
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- W4281567180 cites W1989143971 @default.
- W4281567180 cites W1989810121 @default.
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- W4281567180 cites W1993943341 @default.
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- W4281567180 cites W2010854533 @default.
- W4281567180 cites W2012139691 @default.
- W4281567180 cites W2017496419 @default.
- W4281567180 cites W2022251773 @default.
- W4281567180 cites W2024619129 @default.
- W4281567180 cites W2025105368 @default.
- W4281567180 cites W2025624195 @default.
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- W4281567180 cites W2071991225 @default.
- W4281567180 cites W2076848254 @default.
- W4281567180 cites W2081892602 @default.
- W4281567180 cites W2083244872 @default.
- W4281567180 cites W2089804376 @default.
- W4281567180 cites W2092623245 @default.
- W4281567180 cites W2102838769 @default.
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- W4281567180 cites W2166491004 @default.
- W4281567180 cites W2173181922 @default.
- W4281567180 cites W2198225272 @default.
- W4281567180 cites W2289953168 @default.
- W4281567180 cites W2325816607 @default.
- W4281567180 cites W2326826466 @default.
- W4281567180 cites W2333558806 @default.
- W4281567180 cites W2593377099 @default.
- W4281567180 cites W2616906870 @default.
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- W4281567180 cites W2756367641 @default.
- W4281567180 cites W2764008202 @default.
- W4281567180 cites W2767487674 @default.
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- W4281567180 cites W2889283094 @default.
- W4281567180 cites W2909704931 @default.
- W4281567180 cites W2919363152 @default.
- W4281567180 cites W2950037073 @default.
- W4281567180 cites W2950486495 @default.
- W4281567180 cites W2952297084 @default.
- W4281567180 cites W2952855503 @default.
- W4281567180 cites W2952958258 @default.
- W4281567180 cites W2981915963 @default.
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- W4281567180 doi "https://doi.org/10.3390/catal12060578" @default.
- W4281567180 hasPublicationYear "2022" @default.
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