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- W2764037889 endingPage "6563" @default.
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- W2764037889 abstract "In this study, a one-pot two-step Pd-catalyzed reductive eliminate between acetyl naphthalene derivatives, tosylhydrazide, and aryl halide, affording substituted 1(or 2)-(1-phenylvinyl)naphthalene in moderate-to-excellent yields, was reported. Notably, solvent played a crucial role in the coupling of 1-acetyl naphthalene derivatives (toluene) or 2-acetyl naphthalene derivatives (1, 4-dioxane) as starting materials. Meanwhile, the scope of this one-pot coupling reaction was extended to 1(or 2)-naphthaldehyde substrates. Importantly, the catalytic system can be employed on a wide variety of substrates with good functional group tolerance. This protocol could also be particularly useful for the synthesis of olefins-substituents hydroxyl compounds." @default.
- W2764037889 created "2017-10-20" @default.
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- W2764037889 date "2017-11-01" @default.
- W2764037889 modified "2023-10-17" @default.
- W2764037889 title "Synthesis of naphthyl-substituted terminal olefins via Pd-Catalyzed one-pot coupling of acetylnaphthalene, N -Tosylhydrazide with aryl halide" @default.
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- W2764037889 doi "https://doi.org/10.1016/j.tet.2017.09.052" @default.
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