Issue 1, 1985

Metallacyclobutene formation from a substituted-acetylene complex of cobalt and an isocyanide. Regioselectivity and rearrangement

Abstract

The regioselectivity observed in the formation of the iminocobaltacyclobutenes (3) from the substituted-acetylene complex (1) and the isocyanide (2) has been shown to be due to the electronic effect of substituents on the acetylene; skeletal rearrangement of the metallacycle had proved that the complexes (3) are the kinetically controlled products.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 35-37

Metallacyclobutene formation from a substituted-acetylene complex of cobalt and an isocyanide. Regioselectivity and rearrangement

Y. Wakatsuki, S. Miya, S. Ikuta and H. Yamazaki, J. Chem. Soc., Chem. Commun., 1985, 35 DOI: 10.1039/C39850000035

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