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- W2079269312 abstract "The hydrodehalogenation of alkyl and aryl halides was efficiently performed using a reducing system composed of CuCl2·2H2O, an excess of lithium sand and a catalytic amount (5 mol%) of 4,4′-di-tert-butylbiphenyl (DTBB) as electron carrier, in tetrahydrofuran at room temperature. The reaction of a series of alkyl and aryl fluorides, chlorides, bromides, and iodides with this combination led to the formation of the corresponding products resulting from a halogen/hydrogen exchange. The use of deuterium oxide instead of water in the copper salt allowed the preparation of the corresponding deuterated products." @default.
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- W2079269312 date "2004-09-01" @default.
- W2079269312 modified "2023-09-30" @default.
- W2079269312 title "Hydrodehalogenation of organic halides using the CuCl2·2H2O-Li-arene(cat.) combination" @default.
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- W2079269312 doi "https://doi.org/10.1016/j.apcata.2004.01.038" @default.
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