Copper species highly dispersed on suitable inert oxide supports catalyze the amidation of the alpha-C-H bond of cyclic ethers using a commercial, environmentally benign nitrene source such as chloramine T. The catalytic efficiency depends on the nature of the support and of the dispersed copper species. The heterogeneous catalysts apparently operate by liberating low amounts of highly catalytically active copper species into solution, the exact nature of which is yet to be determined. The heterogeneous catalysts are easily separable and recyclable, although the catalytic activity decreases upon recycling.

Heterogeneous copper-based catalysts for nitrene insertions into C-H bonds

Federica Zaccheria;Nicoletta Ravasio
2013

Abstract

Copper species highly dispersed on suitable inert oxide supports catalyze the amidation of the alpha-C-H bond of cyclic ethers using a commercial, environmentally benign nitrene source such as chloramine T. The catalytic efficiency depends on the nature of the support and of the dispersed copper species. The heterogeneous catalysts apparently operate by liberating low amounts of highly catalytically active copper species into solution, the exact nature of which is yet to be determined. The heterogeneous catalysts are easily separable and recyclable, although the catalytic activity decreases upon recycling.
2013
Istituto di Scienze e Tecnologie Molecolari - ISTM - Sede Milano
CHLORAMINE-T
CONJUGATE ADDITION
COUPLING REACTIONS
AMINATION
ALKYLATION
MECHANISM
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/247815
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