Abstract
The reactivity of 9-chloro-9-phosphaalkenylchloro-9-germafluorene stabilized by the introduction of the germanium atom into a fluorenyl system, was tested in reaction with lithium derivatives as methyllithium, normal-, sec- and tert-butyllithium. The reactions underwent, depending on the used organolithium derivative, either with the alkylation of the germanium atom or through a lithiation of the carbon atom of the phosphaalkenyl unit, and the successive formation of a carbanion through elimination of LiCl followed by the dimerization of this intermediate species.
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