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Isoindolinone synthesis through Rh/Cu-catalyzed oxidative C-H/N-H annulation of N -methoxy benzamides with saturated ketones.

Xiao DuYuntao HuDarun YangDecai HuangWendi YangHailong WuHuai-Qing Zhao
Published in: Organic & biomolecular chemistry (2022)
The synthesis of isoindolinones from N -methoxy benzamides and saturated ketones via a bimetallic tandem catalytic annulation has been accomplished. The reaction is catalyzed by a Rh/Cu-cocatalytic system and proceeds via the combination of Cu-catalyzed dehydrogenation of ketones and Rh-catalyzed direct C-H functionalization with the assistance of the N -methoxy amide group which also acts as an oxidant to regenerate the Rh catalyst. This method shows good compatibility with a wide range of substrates and functional groups, and provides an alternative strategy to obtain diverse isoindolinones.
Keyphrases
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  • aqueous solution
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  • transition metal