Synthesis of an Areno-anellated [3.3.1]Propellane

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Gerald Dyker, Jutta Körning, Peter Bubenitschek and Peter G. Jones


Abstract

The reactivity of a highly strained [3.3.1]propellane 6 is exemplified by the addition of formic acid to the central C–C single bond.


References

  1. K. B. Wiberg, Chem. Rev., 1989, 89, 975 CrossRef CAS.
  2. P. Warner and R. LaRose, Tetrahedron Lett., 1972, 21, 2141 CrossRef.
  3. R. E. Pincock, J. Schmidt, W. B. Scott and E. J. Torupka, Can. J. Chem., 1972, 50, 3958 CAS.
  4. K. Wiberg and G. J. Burgmaier, J. Am. Chem. Soc., 1972, 94, 7396 CrossRef CAS.
  5. I. D. Reingold and J. Drake, Tetrahedron Lett., 1989, 30, 1921 CrossRef CAS.
  6. L. A. Paquette, T. Kobayashi and J. C. Gallucci, J. Am. Chem. Soc., 1988, 110, 1305 CrossRef CAS.
  7. A. Schuster and D. Kuck, Angew. Chem., 1991, 103, 1717 CAS; Angew. Chem., Int. Ed. Engl., 1991, 30, 1699 Search PubMed.
  8. G. Dyker, Tetrahedron Lett., 1991, 32, 7241 CrossRef CAS.
  9. G. Dyker, J. Körning, P. G. Jones and P. Bubenitschek, Angew. Chem., 1993, 105, 1805 CAS; Angew. Chem., Int. Ed. Engl., 1993, 32, 1733 Search PubMed.
  10. S. E. Denmark and J. P. Edwards, J. Org. Chem., 1991, 56, 6974 CrossRef CAS.
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