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The Gomberg-Bachmann Reaction for the Arylation of Anilines with Aryl Diazotates

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Journal Chemistry
Specialty Chemistry
Date 2012 Aug 14
PMID 22887751
Citations 3
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Abstract

Simply aqueous sodium hydroxide is sufficient to exclude ionic side reactions and to prepare 2-aminobiphenyls from aryl diazotates and anilines through a new variant of the Gomberg-Bachmann reaction (see scheme). The metal-free reaction under basic conditions allows to exploit the highly radical-stabilizing effect of the aniline's free amino function for the first time, which leads to a so far unreached regioselectivity.

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