Journal
ORGANOMETALLICS
Volume 32, Issue 21, Pages 6240-6247Publisher
AMER CHEMICAL SOC
DOI: 10.1021/om4004362
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Funding
- EC [CP-FP 211468-2 EUMET]
- Royal Society
- Engineering and Physical Sciences Research Council [GR/S31273/01] Funding Source: researchfish
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The synthesis, characterization, and catalytic activity of two new complexes, 2a,b, featuring a sterically demanding NHC and two different phosphites are described. Complexes 2a,b display a mutually trans arrangement of the pi-acidic phosphite and the strong sigma-donor SIPr ligand (SIPr = N,N'-bis(2,6-diisopropylphenyl)imidazolin-2-ylidene). The synergy between the phosphite and the NHC ligand was revealed in the RCM of challenging substrates leading to tetrasubstituted olefins where, in comparison to their phosphine-containing analogues, 2a,b allowed higher conversions of these challenging substrates.
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