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An efficient method for the synthesis of C -phosphonoketenimines through palladium-catalyzed migratory insertion of isocyanides has been developed for the first time. This procedure tolerates wide functional groups and has a good atom economy. Further transformations of the products, which are useful building blocks for the β-aminophosphonates, β-aminovinylphosphonates, and C -phosphorylated tetrazoles, indicate potential synthetic utility.
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Yang et al. (2016) studied this question.
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