Abstract
The reaction of 2-ferrocenylpyridine with n-butyl-lithium in light petroleum, in tetrahydrofuran, and in NNNN′-tetramethyl-1,2-diaminoethane gave a different range of products in each solvent. The same ferrocene was also metallated by t-butyl-lithium and by methyl-lithium in diethyl ether. Both metallation and addition across the carbon–nitrogen double bond were achieved with the former reagent; the latter behaved only as a metallating agent.

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