Ring-opening Reactions of Cyclopropanes. Part 5.1 Reactivity of Ethyl trans-2,2-Dimethoxy-3-methylcyclopropane-1-carboxylate towards Electrophilic Diazenes

Journal of Chemical Research - Part S

Volumn , Issue 2, 1996, Pages 82-83

  Graziano, M Liliana ^a   Iesce, M Rosaria ^a   Cermola, Flavio ^a  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

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EID: 2742548785     PISSN: 03082342     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (28)

1. Part 4: M. L. Graziano, M. R. Iesce, F. Cermola and G. Cimminiello, J. Chem. Res., 1992, (S) 4; (M) 0157.
2. Part 4: M. L. Graziano, M. R. Iesce, F. Cermola and G. Cimminiello, J. Chem. Res., 1992, (S) 4; (M) 0157.
3. M. L. Graziano and M. R. Iesce, J. Chem. Res., 1987, (S) 362; (M) 2942.
4. M. L. Graziano and M. R. Iesce, J. Chem. Res., 1987, (S) 362; (M) 2942.
5. M. L. Graziano and G. Cimminiello, J. Chem. Res., 1989, (S) 42; (M) 0446.
6. M. L. Graziano and G. Cimminiello, J. Chem. Res., 1989, (S) 42; (M) 0446.
7. M. L. Graziano and S. Chiosi, J. Chem. Res. (S), 1989, 44.
8. Many pyrazolidine derivatives are biologically active. See: J. Elguero, in Comprehensive Heterocyclic Chemistry, ed. A. R. Katritzky and C. W. Rees, Pergamon Press, Oxford, 1984, vol. 5, p. 167; J. F. Bagli, L. J. Lombardo and J. S. Skotnicki, Eur. Pat. Appl., EP 511865/1992 (Chem. Abstr., 1993, 118, 234052a); S. Nishigaki, M. Sakae, M. Katsurada, M. Watabe, T. Sabato, M. Hase and E. Ootsubo, Jpn. Pat Appl., 338958/1990 (Chem Abstr., 1993, 118, 124552f); S. Nishigaki, K. Chiga, M. Sakae, M. Katsurada, S. Ueda, K. Hirata, M. Hase and F. Ninomiya, Jpn. Pat. Appl., 214258/1986 (Chem. Abstr., 1988, 109, 129000y).
9. Many pyrazolidine derivatives are biologically active. See: J. Elguero, in Comprehensive Heterocyclic Chemistry, ed. A. R. Katritzky and C. W. Rees, Pergamon Press, Oxford, 1984, vol. 5, p. 167; J. F. Bagli, L. J. Lombardo and J. S. Skotnicki, Eur. Pat. Appl., EP 511865/1992 (Chem. Abstr., 1993, 118, 234052a); S. Nishigaki, M. Sakae, M. Katsurada, M. Watabe, T. Sabato, M. Hase and E. Ootsubo, Jpn. Pat Appl., 338958/1990 (Chem Abstr., 1993, 118, 124552f); S. Nishigaki, K. Chiga, M. Sakae, M. Katsurada, S. Ueda, K. Hirata, M. Hase and F. Ninomiya, Jpn. Pat. Appl., 214258/1986 (Chem. Abstr., 1988, 109, 129000y).
10. Many pyrazolidine derivatives are biologically active. See: J. Elguero, in Comprehensive Heterocyclic Chemistry, ed. A. R. Katritzky and C. W. Rees, Pergamon Press, Oxford, 1984, vol. 5, p. 167; J. F. Bagli, L. J. Lombardo and J. S. Skotnicki, Eur. Pat. Appl., EP 511865/1992 (Chem. Abstr., 1993, 118, 234052a); S. Nishigaki, M. Sakae, M. Katsurada, M. Watabe, T. Sabato, M. Hase and E. Ootsubo, Jpn. Pat Appl., 338958/1990 (Chem Abstr., 1993, 118, 124552f); S. Nishigaki, K. Chiga, M. Sakae, M. Katsurada, S. Ueda, K. Hirata, M. Hase and F. Ninomiya, Jpn. Pat. Appl., 214258/1986 (Chem. Abstr., 1988, 109, 129000y).
11. Many pyrazolidine derivatives are biologically active. See: J. Elguero, in Comprehensive Heterocyclic Chemistry, ed. A. R. Katritzky and C. W. Rees, Pergamon Press, Oxford, 1984, vol. 5, p. 167; J. F. Bagli, L. J. Lombardo and J. S. Skotnicki, Eur. Pat. Appl., EP 511865/1992 (Chem. Abstr., 1993, 118, 234052a); S. Nishigaki, M. Sakae, M. Katsurada, M. Watabe, T. Sabato, M. Hase and E. Ootsubo, Jpn. Pat Appl., 338958/1990 (Chem Abstr., 1993, 118, 124552f); S. Nishigaki, K. Chiga, M. Sakae, M. Katsurada, S. Ueda, K. Hirata, M. Hase and F. Ninomiya, Jpn. Pat. Appl., 214258/1986 (Chem. Abstr., 1988, 109, 129000y).
12. H. Hogeveen and L. Zwart, J. Org. Chem., 1979, 44, 1365.
13. D. J. Pasto, A. F. T. Chen and G. Binsch, J. Am. Chem. Soc., 1973, 95, 1553; D. J. Pasto and A. F. T. Chen, Tetrahedron Lett., 1972, 2995; 1973, 713.
14. D. J. Pasto, A. F. T. Chen and G. Binsch, J. Am. Chem. Soc., 1973, 95, 1553; D. J. Pasto and A. F. T. Chen, Tetrahedron Lett., 1972, 2995; 1973, 713.
15. D. J. Pasto, A. F. T. Chen and G. Binsch, J. Am. Chem. Soc., 1973, 95, 1553; D. J. Pasto and A. F. T. Chen, Tetrahedron Lett., 1972, 2995; 1973, 713.
16. 11 Moreover, for the not formed trans-isomer of the pyrazolidine 4, the calculated value was 2.1.
17. J. Abraham, J. Fisher and P. Loftus, Introduction to NMR Spectroscopy, Wiley, New York, 1988, p. 43.
18. C. A. G. Haasnoot, F. A. A. M. de Leeuw and C. Altona, Tetrahedron. 1980, 36, 2783.
19. Serena Software, Bloomington, IN, USA.
20. L. M. Jackman and S. Sternhell, Application of Nuclear Magnetic Resonance Spectroscopy in Organic Chemistry, Pergamon Press, Oxford, 1969, p. 291
21. A. J. Fatiadi, Synthesis, 1986, 249.
22. M. L. Graziano and R. Scarpati, J. Chem. Soc., Perkin Trans. 1, 1985, 289.
23. M. L. Graziano and M. R. Iesce, Synthesis, 1985, 762.
24. R. C. Cookson, I. D. R. Stevens and C. T. Watts, Chem. Commun., 1966, 744; R. C. Cookson, S. S. H. Gilani and I. D. R. Stevens, J. Chem. Soc. C, 1967, 1905.
25. R. C. Cookson, I. D. R. Stevens and C. T. Watts, Chem. Commun., 1966, 744; R. C. Cookson, S. S. H. Gilani and I. D. R. Stevens, J. Chem. Soc. C, 1967, 1905.
26. C. J. Moody, Adv. Heterocycl Chem., 1982, 30, 1.
27. For a recent example, see: S. Shimada, Y. Hashimoto, T. Nagashima, M. Hasegawa and K. Saigo, Tetrahedron, 1993, 49, 1589; for a review see: H.-U. Reissig. Top Curr. Chem., 1988, 144, 73.
28. For a recent example, see: S. Shimada, Y. Hashimoto, T. Nagashima, M. Hasegawa and K. Saigo, Tetrahedron, 1993, 49, 1589; for a review see: H.-U. Reissig. Top Curr. Chem., 1988, 144, 73.