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Analogs of Grubbs’ Second Generation Catalyst with Hydrophilic Phosphine Ligands: Phase Transfer Activation of Ring Closing Alkene Metathesis
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Citations
17
References
2011
Year
Inorganic ChemistryEngineeringAlkene MetathesisClosing Alkene MetathesisCatalytic SynthesisOrganic ChemistryHydrophilic PhosphineOrganometallic CatalysisCatalysisSecond Generation CatalystChemistryPhase TransferAsymmetric CatalysisHydrophilic Phosphine LigandsPhase Transfer ActivationBiomolecular Engineering
Analogs of Grubbs' second generation catalyst with hydrophilic phosphine ligands are synthesized, and those with Cy(2)PCH(2)CH(2)N(CH(3))(3)(+) Cl(-) and Cy(2)PCHCH(2)CH(2)N(CH(3))(2)(+)CH(2)CH(2) Cl(-) give much faster ring closing metatheses under CH(2)Cl(2)/aqueous or CH(2)Cl(2)/aqueous HCl biphasic as opposed to CH(2)Cl(2) monophasic conditions. This is attributed to rapid phase transfer of the dissociated ligand to the aqueous phase, where under acidic conditions it is protonated.
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