Collect. Czech. Chem. Commun.
2001, 66, 1521-1528
https://doi.org/10.1135/cccc20011521
Spiro[4.5]deca-2,7-diene-1,6-dione and Spiro[5.5]undeca-2,8-diene-1,7-dione. Synthesis, Reductions and Palladium-Catalyzed Allylic Substitutions
Doina Sirbu* and Valeriu Sunel
Department of Organic Chemistry, "Al. I. Cuza" University of Iasi, Bd. Carol I, 11, 6600 Iasi, Romania
References
1. H., Muller W.: Helv. Chim. Acta 1972, 55, 2277.
<https://doi.org/10.1002/hlca.19720550702>
2. H.: Helv. Chim. Acta 1968, 51, 1587.
<https://doi.org/10.1002/hlca.19680510712>
3. D. J., Van Duuren B. L.: J. Am. Chem. Soc. 1955, 77, 3576.
<https://doi.org/10.1021/ja01618a046>
4. E., Maeder, E., Semarne H. M., Cram D. J.: J. Am. Chem. Soc. 1959, 81, 2729.
<https://doi.org/10.1021/ja01520a034>
5. N., Ai T., Uda H.: J. Chem. Soc., Chem. Commun. 1982, 232.
<https://doi.org/10.1039/c39820000232>
6. M., Kuritani H., Shingu K.: J. Chem. Soc., Chem. Commun. 1977, 812.
<https://doi.org/10.1039/c39770000812>
7. N., Mutal A., Kumar A.: J. Chem. Soc., Chem. Commun. 1992, 493.
<https://doi.org/10.1039/c39920000493>
8. Y., Xue S. Li Z., Deng J., Mi A., Chan A. C.: Tetrahedron: Asymmetry 1998, 9, 3185.
<https://doi.org/10.1016/S0957-4166(98)00339-5>
9. J. A., Parvez M., Keay B. A.: Tetrahedron: Asymmetry 1993, 4, 1973.
<https://doi.org/10.1016/S0957-4166(00)82242-9>
10. M., De Clercq P.: Tetrahedron 1985, 41, 1767.
11. J. M. G., Angers P., Canonne P.: Tetrahedron Lett. 1994, 35, 2849.
<https://doi.org/10.1016/S0040-4039(00)76641-X>
12. D., Falk-Pedersen M.-L., Romming C., Undheim K.: Tetrahedron 1999, 55, 6703.
<https://doi.org/10.1016/S0040-4020(99)00316-6>
13. M. F., Foss J. C., Katz S.: J. Am. Chem. Soc. 1973, 95, 7325.
<https://doi.org/10.1021/ja00803a021>
14. S., Ovadia D.: J. Chem. Soc., Perkin Trans. 1 1974, 333.
<https://doi.org/10.1039/p19740000333>

