Addition of diazocyclopropane generated in situ to acrylic acid derivatives and transformations of resulting functionally substituted spiro(pyrazolinecyclopropanes)

Russian Chemical Bulletin

Volumn 46, Issue 3, 1997, Pages 511-518

  Tomilov, Yu V ^a   Kostyuchenko, I V ^a   Shulishov, E V ^a   Nefedov, O M ^a  

^a N D ZELINSKY INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

Author keywords

1,3 dipolar cycloaddition; NMR spectra; Nucleophilic addition; Spiro(2 pyrazoline 5,1 cyclopropanes); Spiropentanes; Thermolysis

Indexed keywords

EID: 0031530335     PISSN: 10665285     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02495406     Document Type: Article

References (17)

1. M Regitz and H. Heydt, 1,3-Dipolar Cycloaddition Chemistry, Ed. A. Padwa, Wiley Interscience, N.Y., 1984, v. 1, p. 393.
2. C. H. Jarboe, in The Chemistry of Heterocyclic Compounds, Ed. A. Weissberger, Wiley, 1967, 22, 209.
3. N. B. Burmanova, Sovremen. probl. organ. khimii [Modern Problems of Organic Chemistry] Izd. LGU, issue 3, 1974, 150.
4. P. Bladon, D. R. Rae, and A. D. Tait, J. Chem. Soc., Perkin Trans. I, 1974, 1468.
5. P. Bladon and D. R. Rae, J. Chem Soc., Perkin Trans. I, 1974, 2240.
6. Yu. V. Tomilov, E. V. Shulishov, S. A. Yarygin, and O. M. Nefedov, Izv. Akad. Nauk, Ser. Khim., 1995, 2203 [Russ. Chem. Bull., 1995, 44, 2109 (Engl. Transl.)].
7. Yu. V. Tomilov, E. V. Shulishov, S. A. Yarygin, and O. M. Nefedov, Izv. Akad. Nauk, Ser. Khim., 1995, 2203 [Russ. Chem. Bull., 1995, 44, 2109 (Engl. Transl.)].
8. W. M. Jones, M. M. Cirasley, and W. S. Brey, J. Am. Chem. Soc., 1963, 85, 2754.
9. Yu. V. Tomilov, E. V. Shulishov, and O. M. Nefedov, Izv. Akad. Nauk SSSR. Ser. Khim., 1991, 1057 [Bull. Acad. Sci. USSR. Div. Chem. Sci., 1991, 40, 939 (Engl. Transl.)].
10. Yu. V. Tomilov, E. V. Shulishov, and O. M. Nefedov, Izv. Akad. Nauk SSSR. Ser. Khim., 1991, 1057 [Bull. Acad. Sci. USSR. Div. Chem. Sci., 1991, 40, 939 (Engl. Transl.)].
11. Yu. V. Tomilov, E. V. Shulishov, G. P. Okonnishnikova, and O. M. Nefedov, Izv. Akad. Nauk, Ser. Khim., 1995, 2199 [Russ. Chem. Bull., 1995, 44, 2105 (Engl. Transl.)].
12. Yu. V. Tomilov, E. V. Shulishov, G. P. Okonnishnikova, and O. M. Nefedov, Izv. Akad. Nauk, Ser. Khim., 1995, 2199 [Russ. Chem. Bull., 1995, 44, 2105 (Engl. Transl.)].
13. P. S. Engel and D. B. Gerth, J. Am. Chem. Soc., 1983, 105, 6849.
14. G. F. Duffin and J. D. Kendall, J. Chem. Soc., 1954, 408.
15. W. Kirmse and H. Schütte, Chem. Ber., 1968, 101, 1674.
16. P. S. Engel and D. B. Gerth, J. Am. Chem. Soc., 1981, 103, 7689; H. J. Rosenkranz and H. Schmid, Helv. Chim. Acta, 1968, 51, 1628.
17. P. S. Engel and D. B. Gerth, J. Am. Chem. Soc., 1981, 103, 7689; H. J. Rosenkranz and H. Schmid, Helv. Chim. Acta, 1968, 51, 1628.