257300-22-4

Upstream product

• 172162-31-1 (μ-η3-PhCCCH2)(μ-Cl)Pd2(triphenylphosphine)2 
• 603-35-0 triphenylphosphine 

Downstream Products

• 166939-88-4 Pd(P(C₆H₅)3)2(CH₂CHCHC₆H₅)⁽¹⁺⁾*B(C₆H₅)4^(1-)=[Pd(P(C₆H₅)3)2(CH₂CHCHC₆H₅)]B(C₆H₅)4 
• 172162-31-1 (μ-η3-PhCCCH2)(μ-Cl)Pd2(triphenylphosphine)2 
• 257300-29-1 Pd(C₆H₅CCCH₂)(P(C₆H₅)3)2⁽¹⁺⁾*B(C₆H₅)4^(1-) = [Pd(C₆H₅CCCH₂)(P(C₆H₅)3)2]B(C₆H₅)4 
• 172162-34-4 (μ-η3-PhCCCH2)(μ-I)Pd2(triphenylphosphine)2 
• 172162-35-5 (μ-η3-PhCCCH2)(μ-SPh)Pd2(triphenylphosphine)2 
• 340703-92-6 (C₆H₅CC(COCH₃)CH₂)PdCl(P(C₆H₅)3)Pd(Cl)(P(C₆H₅)3) 
• 340703-99-3 (μ-η3-PhCCCH2)(μ-Br)Pd2(triphenylphosphine)2 

Relevant academic research and scientific papers

Carbon-carbon bond formation by electrophilic addition at the central carbon of the μ-η3-allenyl/propargyl ligand on the Pd-Pd bond

The μ-η3-allenyl/propargyldipalladium complexes were synthesized by the reaction of the corresponding η1-allenyl- or η1-propargylpalladium complexes with Pd2(dba)3. The X-ray diffraction analysis indi