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• W2118740852 startingPage "7481" @default.
• W2118740852 abstract "Abstract A Rh III ‐catalysed ortho C–H amination of phenidones under mild conditions was developed using N ‐alkyl‐ O ‐benzoyl‐hydroxylamines as aminating agents, and with a cyclic hydrazine moiety as a directing group, yields of up to 97 % and a high functional group tolerance were observed. This strategy offers an alternative route for the synthesis of amino analogues of the 5‐lipoxygenase inhibitor phenidone, and the products are valuable for further functional group transformations." @default.
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• W2118740852 date "2014-10-09" @default.
• W2118740852 modified "2023-10-12" @default.
• W2118740852 title "Rh^III-Catalysed Hydrazine-Directed C(sp²)-H Amination of Phenidones with<i>N</i>-Alkyl-<i>O</i>-benzoyl-hydroxylamines" @default.
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• W2118740852 doi "https://doi.org/10.1002/ejoc.201402999" @default.
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