Publication | Closed Access
A Zirconium Promenade - An Efficient Tool in Organic Synthesis
56
Citations
0
References
2006
Year
Chemical EngineeringZirconium PromenadeEngineeringOne-pot PreparationEnol Ether DerivativesCross-coupling ReactionNatural SciencesDiversity-oriented SynthesisSustainable SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisCarbon TetherChemistrySynthesis MethodSynthetic ChemistryBiomolecular Engineering
The one-pot preparation of allyl- and dienyl-zirconocene derivatives can be easily achieved via a tandem allylic C-H-activation-β-elimination reaction from unsaturated fatty alcohol and enol ether derivatives, respectively. The reaction proceeds rapidly, under mild conditions, and is insensitive to the length of the carbon tether between the double bond and the leaving group moiety.