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Ruthenium Catalyst for the meta-Selective Substitution Reaction
(p-Cymene)bis(mesitylcarboxylato)ruthenium(II) (1), a ruthenium complex used to catalyze C-H bond functionalizations has been recently reported by Ackermann et al. In the presence of catalytic amounts of 1, substituted benzene derivatives are regioselectively alkylated at the meta-position by treatment with secondary alkyl halides in good yield.1) Furthermore, when o-alkylbenzoic acid derivatives are treated with alkenes and the catalyst 1, meta-alkenylated arenes are provided via decarboxylative C-H bond activation.2) In addition, 1 is effective at C(sp3)-H activation of benzylamine derivatives.3) 1 can be used as a catalyst for various types of aryl functionalization through C-H bond activation.
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References
- 1)meta-Selective C-H Bond Alkylation with Secondary Alkyl Halides
- 2)Ruthenium(II)-Catalyzed Decarboxylative C-H Activation: Versatile Routes to meta-Alkenylated Arenes
- 3)C(sp3)-H Bond Arylations Catalyzed by Well-Defined [Ru(O2CMes)2(p-cymene)]