Asymmetric hydrogenation of alkenes lacking coordinating groups
Asymmetric hydrogenation of olefins is one of the most important reactions for the synthesis of optically active compounds, especially in industry. Chiral iridium catalysts based on P,N ligands have strongly expanded their application range. In contrast to rhodium and ruthenium diphosphine complexes...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2011-07, Vol.47 (28), p.7912-7916 |
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container_title | Chemical communications (Cambridge, England) |
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creator | Woodmansee, David H Pfaltz, Andreas |
description | Asymmetric hydrogenation of olefins is one of the most important reactions for the synthesis of optically active compounds, especially in industry. Chiral iridium catalysts based on P,N ligands have strongly expanded their application range. In contrast to rhodium and ruthenium diphosphine complexes they do not require the presence of a coordinating group near the C=C bond and, therefore, allow highly enantioselective hydrogenations of largely unfunctionalized alkenes. |
doi_str_mv | 10.1039/c1cc11430a |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Alkenes Asymmetry Bonding Hydrogenation Ligands Optical activity Rhodium Ruthenium |
title | Asymmetric hydrogenation of alkenes lacking coordinating groups |
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