Abstract

Catalytic cyclotrimerization of acetylenic compounds by transient complexes formed in the reduction of nickel halides by magnesium, occurs with many alkynes; however, this cyclization is hindered when bulky groups are close neighbors of the triple bond or when acceptor groups are in the α position with respect to the unsaturated carbon. On the other hand, the yield of trimer increases to become quantitative with releasing substituents.

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