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Wiley, ChemCatChem, 9(3), p. 1496-1502, 2011

DOI: 10.1002/cctc.201100076

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A Palladium-Catalyzed Multicascade Reaction: Facile Low- Temperature Hydrogenolysis of Activated Nitriles and Related Functional Groups

This paper is available in a repository.
This paper is available in a repository.

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Abstract

The facile hydrogenolysis of various nitriles, imines, and amines over Pd/C has been achieved by using straightforward and relatively mild conditions. Substrates that contain an aryl group adjacent to the nitrogen-containing functionality were hydrogenolyzed most effectively. The stabilization of the proposed h2-coordinated palladium intermediate by this group was partly responsible for this observation and is borne out by ab initio calculations.