Collect. Czech. Chem. Commun.
2004, 69, 231-241
https://doi.org/10.1135/cccc20040231
Quantum-Chemical Insight Into Mechanism of Combined Intra-Intermolecular Cycloaddition
Petr Kulháneka,b, Milan Potáčekb and Jaroslav Kočaa,b,*
a National Centre for Biomolecular Research, Faculty of Science, Masaryk University Brno, Kotlářská 2, CZ-611 37 Brno, Czech Republic
b Department of Organic Chemistry, Faculty of Science, Masaryk University Brno, Kotlářská 2, CZ-611 37 Brno, Czech Republic
References
1. J. Am. Chem. Soc. 1917, 39, 279.
< J. R., Moore N. H.: https://doi.org/10.1021/ja02247a011>
2. Angew. Chem., Int. Ed. Engl. 1974, 86, 474.
< K., Thenn W., Gieren A.: https://doi.org/10.1002/anie.197404741>
3. Heterocycles 1990, 31, 883.
< M., Myiadai S.: https://doi.org/10.3987/COM-90-5351>
4. Lang S., Schantl J. G.: Presented at the 12th Symposium on Chemistry of Heterocyclic Compounds, Brno 1996, P85.
5. J. Org. Chem. 1994, 59, 8003.
< B., Miranda M., Pérez-Castells J., Polanco C., Sierra M. A.: https://doi.org/10.1021/jo00105a014>
6. Tetrahedron Lett. 2002, 43, 4833.
< J., Taraba J., Potáček M.: https://doi.org/10.1016/S0040-4039(02)00893-6>
7a. Tetrahedron Lett. 1993, 34, 51.
< M., Marek R., Žák Z., Trottier J., Janoušek Z., Viehe H. G.: https://doi.org/10.1016/S0040-4039(00)61426-0>
7b. Tetrahedron Lett. 1993, 34, 8341.
< M., Marek R., Žák Z., Trottier J., Janoušek Z., Viehe H. G.: https://doi.org/10.1016/S0040-4039(00)61426-0>
8. J. Chem. Soc., Perkin Trans. 1 1975, 2479.
< S., Suschitzki H.: https://doi.org/10.1039/p19750002479>
9. J. Org. Chem. 1987, 52, 2277.
< T., Hayashi Y., Miki M., Teramura K.: https://doi.org/10.1021/jo00387a031>
10. Tetrahedron Lett. 2002, 43, 6431.
< S., Kulhánek P., Potáček M., Nečas M.: https://doi.org/10.1016/S0040-4039(02)01378-3>
11. Frisch M. J., Trucks G. W., Schlegel H. B., Scuseria G. E., Robb M. A., Cheeseman J. R., Zakrzewski V. G., Montgomery J. A., Stratmann R. E., Jr., Burant J. C., Dapprich S., Millam J. M., Daniels A. D., Kudin K. N., Strain M. C., Farkas O., Tomasi J., Barone V., Cossi M., Cammi R., Mennucci B., Pomelli C., Adamo C., Clifford S., Ochterski J., Petersson G. A., Ayala P. Y., Cui Q., Morokuma K., Malick D. K., Rabuck A. D., Raghavachari K., Foresman J. B., Cioslowski J., Ortiz J. V., Baboul A. G., Stefanov B. B., Liu G., Liashenko A., Piskorz P., Komaromi I., Gomperts R., Martin R. L., Fox D. J., Keith T., Al-Laham C. Y., Peng A., Nanayakkara M., Challacombe P. M. W., Gill B., Johnson W., Chen M. A., Wong M. W., Andres J. L., Gonzalez C., Head-Gordon M., Replogle E. S., Pople J. A.: Gaussian 98, Revision A.9. Gaussian Inc., Pittsburgh (PA) 1998.
12. J. Chem. Phys. 1993, 98, 5648.
< A. D.: https://doi.org/10.1063/1.464913>
13. Phys. Rev. B: Condens. Matter 1988, 37, 785.
< C., Yang W., Parr R. G.: https://doi.org/10.1103/PhysRevB.37.785>
14. Chem. Phys. Lett. 1989, 157, 200.
< B., Savin A., Stoll H., Preuss H.: https://doi.org/10.1016/0009-2614(89)87234-3>
15. Flükiger P., Lüthi H. P., Portmann S., Weber J.: MOLEKEL 4.0. Swiss Center for Scientific Computing, Manno (Switzerland) 2000.