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The dialkylation and dideuteration of cyanides are proposed to proceed through intermediates of the type RR′CHCN · LiR″. The title compound 1 (central framework shown on the right) is the first structurally characterized compound of this type. The results of ab initio calculations on the model compound H3CCN · LiNH2 are in agreement with the high stability and the energetically favorable intramolecular proton shift found experimentally.
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Boche et al. (1993) studied this question.
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