Unsymmetrical Ru-NHC catalysts: a key for the selective tandem Ring Opening-Ring Closing alkene Metathesis (RO-RCM) of cycloocteneElectronic supplementary information (ESI) available: Synthesis procedures, characterizations, catalytic reactivity test, X-ray crystal structure analysis. See DOI: 10.1039/c1dt11643f

Dissymmetry for selectivity: NHC ligand with two different pendant group allows the selective formation of cyclic oligomers in place of polymers opening new strategy to generate macrocycles. Dissymmetric NHC ligands on G-II type catalysts allow the selective formation of cyclic oligomers in place of...

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Hauptverfasser: Kavitake, Santosh, Samantaray, Manoja K, Dehn, Richard, Deuerlein, Stephan, Limbach, Michael, Schachner, Jörg A, Jeanneau, Erwan, Copéret, Christophe, Thieuleux, Chloé
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Sprache:eng
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Zusammenfassung:Dissymmetry for selectivity: NHC ligand with two different pendant group allows the selective formation of cyclic oligomers in place of polymers opening new strategy to generate macrocycles. Dissymmetric NHC ligands on G-II type catalysts allow the selective formation of cyclic oligomers in place of polymers.
ISSN:1477-9226
1477-9234
DOI:10.1039/c1dt11643f