A novel synthesis of 2,6-disubstituted and 2,3,6-trisubstituted anilines

DOI: 10.1016/0040-4039(91)80473-J

Source and publish data:

Tetrahedron Letters p. 7191 - 7194 (1991)

Update date:2022-08-29

Topics:

Authors:

Pews Pews

Hunter Hunter

Wehmeyer

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Article abstract of DOI:10.1016/0040-4039(91)80473-J

2,6-Disubstituted and 2,3,6-trisubstituted anilines have been synthesized by a four-step approachy involving the selective reduction of a para halogen of the diacetanilide derivatives utilizing a palladium-on-carbon catalyst and formic acid salts as the in situ hydrogen donor.

Full text of DOI:10.1016/0040-4039(91)80473-J

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