Abstract
The ubiquitous half-sandwich iron complex [CpFe(CO)2Me] (Cp=η5-C5H5) appears to be a catalyst for α-phosphinidene elimination from primary phosphines. Dehydrocoupling reactions provided initial insight into this unusual reaction mechanism, and trapping reactions with organic substrates gave products consistent with an α elimination mechanism, including a rare example of a three-component reaction. The substrate scope of this reaction is consistent with generation of a triplet phosphinidene. In all, this study presents catalytic phosphinidene transfer to unsaturated organic substrates.
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Pagano, J. K., Ackley, B. J., & Waterman, R. (2018). Evidence for Iron-Catalyzed α-Phosphinidene Elimination with Phenylphosphine. Chemistry - A European Journal, 24(11), 2554–2557. https://doi.org/10.1002/chem.201704954
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