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Ozonides from the Ozonolyses of Indene

  • Published : 1999.12.20

Abstract

Ozonolysis reactions of indene 5 in the presence of carbonyl compounds 6 provided the corresponding indenemonoozonide 9 and cross-ozonides 10a-c and 11a-c. Further reactions of ozonides 10 and 11 with the independently prepared carbonyl oxide 13 gave diozonides of structure 14a-c and 15a-c.

Keywords

References

  1. J. Am. Chem. Soc. v.106 Miura, M.;Nojima, M.;Kusabayashi, S.;McCullough, K. J.
  2. J. Org. Chem. v.50 Miura, M.;Fujisaka, T.;Nojima, M.;Kusabayashi, S.;McCullough, K. J.
  3. J. Am. Chem. Soc. v.111 Nakamura, N.;Fujisaka, T.;Nojima, M.;Kusabayashi, S.;McCullough, K. J.
  4. J. Org. Chem. v.58 Sugimoto, T.;Teshima, K.;Nakamura, N.;Nojima, M.;McCullough, K. J.
  5. J. Org. Chem. v.63 Kawamura, S. -I.;Takeuchi, R.;Masuyama, A.;Nojima, M.;McCullough, K. J.
  6. J. Am. Chem. Soc. v.79 Warnell, J. L.;Shriner, R. L.
  7. Justus Liebigs Ann. Chem. v.583 Criegee, R.;Blust, G.;Lohaus, G.
  8. Bull. Korean Chem. Soc. v.20 no.7 Shin, H. S.;Huh, T. S.
  9. Liebigs Ann. Griesbaum, K.;Liu, X.;Kassiaris, A.;Scherer, M.
  10. Liebigs Ann. Griesbaum, K.;Ovez, B.;Huh, T. S.;Dong, Y.
  11. Chem. Ber. v.108 Criegee, R.
  12. Chem. Ber. v.122 Griesbaum, K.;Kiesel, G.
  13. J. Am. Chem. Soc. v.87 Murray, R. W.;Youssefyeh, R. W.;Story, P. R.
  14. Bull. Korean Chem. Soc. v.19 no.11 Huh, T. S.
  15. Chem. Ber. v.122 Griesbaum, K.;Volpp, W.;Huh, T. S.;Jung, I. C.
  16. Can. J. Chem. v.45 Fliszar, S.;Belzecki, Cz.;Cheylinska, J. B.