Palladium-catalyzed coupling reaction of 4-alkylnitrobenzenes with aryl bromides at their benzylic position

DOI: 10.1016/S0040-4039(98)00832-6

Source and publish data:

Tetrahedron Letters p. 4673 - 4676 (1998)

Update date:2022-07-29

Topics:

Authors:

Inoh, Jun-Ichi

Satoh, Tetsuya

Pivsa-Art, Sommai

Miura, Masahiro

Nomura, Masakatsu

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Article abstract of DOI:10.1016/S0040-4039(98)00832-6

4-Alkylnitrobenzenes effectively undergo coupling with aryl bromides at their benzylic position in the presence of a palladium catalyst and a base to give the corresponding mono- and/or di-arylated products in good yields.

Full text of DOI:10.1016/S0040-4039(98)00832-6

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