Synthesis of heterocycle-annelated naphthyridones with a bridgehead nitrogen atom

References

  1. A. G. Nemazanyi, Y. M. Volovenko, T. A. Silaeva and F. S. Babichev, Dokl. Akad. Nauk SSSR, 310, 1990, 1135; Chem. Abstr., 1990, 113, 78221u.
  2. V. Carelli, M. Cardellini and F. Liberatore, Ann. Chim. (Rome), 1959, 49, 709.
  3. R. A. B. Copeland and A. R. Day, J. Am. Chem. Soc., 1943, 65, 1072.
  4. J. Büchi, H. Zwicky and A. Aebi, Arch. Pharm. (Weinheim), 1960, 293, 758.
  5. K. Saito, S. Kambe, Y. Nakano, A. Sakurai and H. Midorikawa, Synthesis, 1983, 210.
  6. G. R. Newkome and C. R. Marston, Tetrahedron, 1983, 39, 2001.
  7. G. Lhommet, H. Sliwa and P. Maitte, Bull. Soc. Chim. Fr., 1972, 1435.
  8. H. Sliwa, Bull. Soc. Chim. Fr., 1970, 631.
  9. Compound 14 has been described previously as an intermediate in the synthesis of allomatridine [10].
  10. S. Okuda, Pharm. Bull (Tokyo), 1957, 5, 462; Chem. Abstr., 52, 1958, 14629e.
  11. K. Palat, L. Novacek and M. Celadnik, Coll. Czech. Chem. Commun., 1967, 32, 1191.
  12. J. V. Dejardin and C. L. Lapière, Bull. Soc. Chim. Fr., 1976, 530.
  13. F. S. Babichev, Y. M. Volovenko, A. G. Nemazanyi and S. I. Tyukhtenko, Ukr. Khim. Zh., 1986, 52, 506; Chem. Abstr., 1987, 107, 7092t.
  14. Y. M. Volovenko, A. G. Nemazanyi and F. S. Babichev, Dopov. Akad. Nauk Ukr. RSR, Ser. B, 1984, 33; Chem. Abstr., 1984, 101, 38376u.
  15. The possible tautomerism of compound 21 was not investigated; the representation as the 3H tautomer was chosen arbitrarily.
  16. A. G. Nemazanyi, Y. M. Volovenko, T. A. Silaeva, M. Y. Kornilov and F. S. Babichev, Khim. Geterotsikl. Soedin., 1992, 86; Chem. Abstr., 1993, 118, 254721w.

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