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- W2225744015 abstract "A mild and efficient palladium-catalyzed synthetic method for the CH functionalization of N-(quinolin-8-yl)ferrocenecarboxamide has been developed. Various aryl iodides containing I, NO2, CN, COMe, CO2Et, and NH functionalities and also alkyl iodides underwent the Pd-catalyzed intermolecular carbon-carbon bond forming reaction with ferrocenecarboxamide successfully which led to a diverse array of bis(aryl/alkyl)ferrocenecarboxamides in 34–92% yields. Cross-coupling of the ferrocenyl CH bond with aryl iodides can also be achieved utilizing an economical Ni catalyst. Additionally, selective monoalkylation of ferrocenecarboxamide was studied using sodium bicarbonate as base and dibenzylphosphoric acid as additive under Pd-catalyzed reaction conditions. Subsequently, removal of the directing group, 8-aminoquinoline, from bis(aryl)ferrocenecarboxamides led to bis(aryl)ferrocenes bearing versatile methyl ester and carboxaldehyde functional groups." @default.
- W2225744015 created "2016-06-24" @default.
- W2225744015 creator A5016203593 @default.
- W2225744015 creator A5022339470 @default.
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- W2225744015 creator A5041944543 @default.
- W2225744015 creator A5047558141 @default.
- W2225744015 creator A5048002686 @default.
- W2225744015 date "2016-01-05" @default.
- W2225744015 modified "2023-10-03" @default.
- W2225744015 title "Palladium‐Catalyzed CH Functionalization of Ferrocenecarboxylic Acid by using 8‐Aminoquinoline as a Removable Directing Group" @default.
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- W2225744015 doi "https://doi.org/10.1002/adsc.201500791" @default.
- W2225744015 hasPublicationYear "2016" @default.
- W2225744015 type Work @default.