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Rhodium- and Iridium-Catalyzed Oxidative Coupling of Benzoic Acids with Alkynes via Regioselective C−H Bond Cleavage

The Journal of Organic Chemistry · 2007 · Vol. 72(14) · pp. 5362–5367
Kenji UeuraTetsuya SatohMasahiro Miura

Abstract

The oxidative coupling of benzoic acids with internal alkynes effectively proceeds in the presence of [Cp*RhCl2]2 and Cu(OAc)2 x H2O as catalyst and oxidant, respectively, to produce the corresponding isocoumarin derivatives. The copper salt can be reduced to a catalytic quantity under air. Interestingly, by using [Cp*IrCl2]2 in place of [Cp*RhCl2]2, the substrates undergo 1:2 coupling accompanied by decarboxylation to afford naphthalene derivatives exclusively. In this case, Ag2CO3 acts as an effective oxidant.

Catalytic C–H Functionalization MethodsOxidative Organic Chemistry ReactionsSynthesis and Catalytic ReactionsChemistryIsocoumarinRegioselectivityIridiumDecarboxylationCatalysisRhodiumMedicinal chemistryOxidative coupling of methaneBond cleavage
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Rhodium- and Iridium-Catalyzed Oxidative Coupling of Benzoic Acids with Alkynes via Regioselective C−H Bond Cleavage · Scinovex