Coupling two multistep catalytic cycles for the one-pot synthesis of propargylamines from alcohols and primary amines on nanoparticulated gold catalyst

Handle

https://riunet.upv.es/handle/10251/29577

Cita bibliográfica

Corma Canós, A.; Navas Escrig, J.; Sabater Picot, MJ. (2012). Coupling two multistep catalytic cycles for the one-pot synthesis of propargylamines from alcohols and primary amines on nanoparticulated gold catalyst. Chemistry - A European Journal. 18(44):14150-14156. https://doi.org/10.1002/chem.201201837

Titulación

Resumen

[EN] A one-pot reaction was performed with a nanoparticulated gold catalyst. A secondary amine is formed through N-monoalkylation of a primary amine with an alcohol by a borrowing hydrogen methodology in a three-step reaction. The secondary amine formed enters into a second A3-coupling cycle to give propargylamines. The multistep reaction requires a gold species formed and stabilized on a ceria surface.

Fuente

Chemistry - A European Journal issn: 0947-6539

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