Nucleophilic reactivity of 1-zirconacyclopent-3-ynes: Carbon–carbon bond formation with aldehydes

Nucleophilic reactions of 1,1-bis(η5-cyclopentadienyl)-1-zirconacyclopent-3-yne (1) with proton and aldehydes were studied. The reaction with HCl gave a mixture of 2-butyne and 1,2-butadiene. Complex 1 reacted with benzaldehyde to give 1-phenyl-2-methyl-2,3-butadien-1-ol (3) in moderate yields in the presence of a proton source such as triethylammonium hydrochloride, while it gave 2-methylene-1-phenyl-3-buten-1-ol (4) on using triethylammonium tetraphenylborate.

1-Zirconacylopent-3-yne (1), a stable five-membered cycloalkyne, reacted with aldehydes in the presence of proton sources to give allenylated and/or dienylated alcohol.Figure optionsDownload as PowerPoint slide