From Wikipedia, the free encyclopedia

The metal ion-catalyzed σ-bond rearrangement is a collection of chemical reactions that occur with highly strained organic compounds are treated with metal ions like Ag+, Rh(I), or Pd(II) based reagents. [1] [2+2] ring openings are sometimes observed:

Scheme 1. Metal-ion-catalyzed σ-bond rearrangement

These rearrangements proceed via oxidative addition of strained rings. Such processes are related to the activation of cyclopropanes by transition metals.

See also

References

  1. ^ Michael B. Smith, Jerry March, March's Advanced Organic Chemistry, 5th Ed., John Wiley & Sons, Inc., 2001, p. 1459. ISBN  0-471-58589-0
From Wikipedia, the free encyclopedia

The metal ion-catalyzed σ-bond rearrangement is a collection of chemical reactions that occur with highly strained organic compounds are treated with metal ions like Ag+, Rh(I), or Pd(II) based reagents. [1] [2+2] ring openings are sometimes observed:

Scheme 1. Metal-ion-catalyzed σ-bond rearrangement

These rearrangements proceed via oxidative addition of strained rings. Such processes are related to the activation of cyclopropanes by transition metals.

See also

References

  1. ^ Michael B. Smith, Jerry March, March's Advanced Organic Chemistry, 5th Ed., John Wiley & Sons, Inc., 2001, p. 1459. ISBN  0-471-58589-0

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