ArticleOrganic letters2015
Cobalt-promoted dimerization of aminoquinoline benzamides.
Article in Organic letters, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Mechanistic Investigations of Cobalt-Catalyzed, Aminoquinoline-Directed C(spJournal of the American Chemical Society · 2025Article
- Palladium-Catalyzed Arylation of C(spACS omega · 2021Article
- Insights into Cobalta(III/IV/II)-Electrocatalysis: Oxidation-Induced Reductive Elimination for Twofold C-H Activation.Angewandte Chemie (International ed. in English) · 2020Article
- Mechanistic details of the cobalt-mediated dehydrogenative dimerization of aminoquinoline-directed benzamides.Chemical science · 2020Article
- Theoretical study of rhodium(III)-catalyzed synthesis of benzoxepine and coumarin.Journal of molecular modeling · 2020Article
- Co-catalyzedRSC advances · 2019Article
- Asymmetric δ-Lactam Synthesis with a Monomeric Streptavidin Artificial Metalloenzyme.Journal of the American Chemical Society · 2019Article
- A comprehensive overview of directing groups applied in metal-catalysed C-H functionalisation chemistry.Chemical Society reviews · 2018Review
- Aminoquinoline-directed, cobalt-catalyzed carbonylation of sulfonamide spChemical communications (Cambridge, England) · 2017Article
- Cobalt-Catalyzed, Aminoquinoline-Directed Functionalization of Phosphinic Amide spACS catalysis · 2016Article
- Cobalt(III)-Catalyzed C-H Bond Amidation with Isocyanates.Organic letters · 2015Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
A method for aminoquinoline-directed, cobalt-promoted dimerization of benzamides has been developed. Reactions proceed in ethanol solvent in the presence of Mn(OAc)2 cocatalyst and Na2CO3 base and use oxygen as a terminal oxidant. Bromo, iodo, nitro, ether, and ester moieties are compatible with the reaction conditions. Cross-coupling of electronically dissimilar aminoquinoline benzamides proceeds with modest yields and selectivities.
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