Methoxymethyl ethers. An activating group for rapid and regioselective metalation

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References (11)

  • J.M. Mallan et al.

    Chem Reviews

    (1969)
  • D.A. Shirely et al.

    J. Organometallic Chem.

    (1968)
    D.A. Shirely et al.

    J. Organometallic Chem.

    (1968)
    R.A. Finnegan et al.

    J. Organometallic Chem.

    (1967)
  • H. Christensen

    Synthetic Comm.

    (1975)
  • R.A. Ellison et al.

    JOC

    (1973)
There are more references available in the full text version of this article.

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