Alkynyldichlorogalliums are Unstable in Hydrocarbon Solvents Dimerization of Alkynyldichlorogalliums via Carbogallation

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Reactivity of permethylscandocene derivatives with acetylene. Structure of acetylenediylbis(permethylscandocene), (.eta.5-C5Me5)2ScC.tplbond.CSc(.eta.5-C5Me5)2Original Research · 1991 · 73 citations
2. 2Regio- and stereocontrolled dimerization of tert-butylacetylene to (Z)-1,4-di-tert-butylbutatriene by ruthenium catalysis. Reaction mechanism involving alkynyl-vinylidene coupling and rearrangement of the metal-bound C4 unitOriginal Research · 1991 · 253 citations
3. 3Synthesis and Properties of Cationic Hydrido(tertiary phosphine)ruthenium(II) ComplexesOriginal Research · 1994 · 57 citations
4. 4Carbometalation of ketone enolates with 1-alkynes: an alkylidenation reaction of silyl enol ethers promoted by stannic chloride-tri-n-butylamine (SnCl4-Bu3N) reagentOriginal Research · 1993 · 39 citations
5. 5Regio- and Stereoselective Dimerization of Phenylacetylene to (Z)-1,4-Diphenylbut-3-en-1-yne by Ruthenium(II) Catalysis. Reaction Mechanism Involving Intermolecular Protonation of .sigma.-Alkynyl by 1-AlkyneOriginal Research · 1994 · 149 citations