Frustrated Lewis Pair Catalyzed Hydrogenations

Jan Paradies

doi:10.1055/s-0032-1318312

Synlett, Table of Contents

Synlett 2013; 24(7): 777-780
DOI: 10.1055/s-0032-1318312

synpacts

Frustrated Lewis Pair Catalyzed Hydrogenations

Authors

Jan Paradies*

Karlsruhe Institute of Technology (KIT), Institute for Organic Chemistry, Fritz-Haber-Weg 6, 76131 Karlsruhe, Germany Fax: +49(721)60848581 Email: jan.paradies@kit.edu

Abstract

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Abstract

The frustrated Lewis pair (FLP) catalyzed hydrogenation of organic molecules is discussed. The saturation of polarized double bonds by FLP can be described as the nucleophilic addition of hydrides to the polar double bond prior to proton transfer. In contrast, the hydrogenation of olefins proceeds first by protonation forming a transient carbocation, which is subsequently attacked by the hydride. Both processes give rise for efficient conversion of unsaturated organic compounds by a metal-free methodology employing molecular hydrogen.

Key words

frustrated Lewis pair - hydrogen activation - hydrogenation - imine - silyl enol ether - olefin

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References

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