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Issue 11, 1987
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Synthesis, stereochemistry, mechanisms of formation, and X-ray crystal structures of enantiomerically pure π-allylpalladium compounds formed via palladium-promoted ring opening of bicyclic alkenes

Abstract

The synthesis, stereochemistry, mechanisms of formation, and X-ray crystal structures of enantiomerically pure π-allylpalladium compounds (1)–(3) prepared by palladium hydride addition to (1R)-(+)-α-pinene, (1S)-(–)-α- or -β-pinene, and (1S)-(+)-2- or -3-carene respectively are presented.

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Article type: Paper
DOI: 10.1039/C39870000834
Citation: J. Chem. Soc., Chem. Commun., 1987,0, 834-836
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    Synthesis, stereochemistry, mechanisms of formation, and X-ray crystal structures of enantiomerically pure π-allylpalladium compounds formed via palladium-promoted ring opening of bicyclic alkenes

    R. C. Larock, H. Song, S. Kim and R. A. Jacobson, J. Chem. Soc., Chem. Commun., 1987, 0, 834
    DOI: 10.1039/C39870000834

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