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Formal arylation of NH3 to produce diphenylamines over supported Pd catalystsElectronic supplementary information (ESI) available: Experimental details, data of diphenlylamine products, Tables S1-S5, and Fig. S1-S6. See DOI: 10.1039/c7cc06737b

In the presence of supported Pd nanoparticle catalysts, e.g. , Pd/Al 2 O 3 , various diphenylamines could be synthesized through acceptorless formal arylation using NH 3 or its surrogates, e.g. , urea, as nitrogen sources and cyclohexanones as arylation sources. The observed catalysis was truly hete...

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Bibliographic Details
Main Authors: Koizumi, Yu, Taniguchi, Kento, Jin, Xiongjie, Yamaguchi, Kazuya, Nozaki, Kyoko, Mizuno, Noritaka
Format: Article
Language:English
Online Access:Get full text
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Summary:In the presence of supported Pd nanoparticle catalysts, e.g. , Pd/Al 2 O 3 , various diphenylamines could be synthesized through acceptorless formal arylation using NH 3 or its surrogates, e.g. , urea, as nitrogen sources and cyclohexanones as arylation sources. The observed catalysis was truly heterogeneous, and the catalyst was reusable with retention of its high catalytic performance. In the presence of Pd/Al 2 O 3 , various diphenylamines could be synthesized through acceptorless formal arylation using urea as a nitrogen source and cyclohexanones as arylation sources.
ISSN:1359-7345
1364-548X
DOI:10.1039/c7cc06737b