Collect. Czech. Chem. Commun. 2007, 72, 1014-1024
https://doi.org/10.1135/cccc20071014

Improved Protocols for Microwave-Assisted Cu(I)-Catalyzed Huisgen 1,3-Dipolar Cycloadditions

Pedro Cintasa, Katia Martinab, Bruna Robaldob, Davide Garellab, Luisa Boffab and Giancarlo Cravottob,*

a Departamento de Química Orgánica, Facultad de Ciencias, Universidad de Extremadura, Avenida de Elvas s/n, E-06071 Badajoz, Spain
b Dipartimento di Scienza e Tecnologia del Farmaco, Università di Torino, Via P. Giuria 9, I-10125 Torino, Italy

References

1a. Kolb H. C., Finn M. G., Sharpless K. B.: Angew. Chem. 2001, 113, 2056. <https://doi.org/10.1002/1521-3757(20010601)113:11<2056::AID-ANGE2056>3.0.CO;2-W>
1b. Kolb H. C., Finn M. G., Sharpless K. B.: Angew. Chem., Int. Ed. 2001, 40, 2004. <https://doi.org/10.1002/1521-3773(20010601)40:11<2004::AID-ANIE2004>3.0.CO;2-5>
1c. Bock V. D., Hiemstra H., van Maarseveen J. H.: Eur. J. Org. Chem. 2006, 51. <https://doi.org/10.1002/ejoc.200500483>
2. Huisgen R. in: 1,3-Dipolar Cycloaddition Chemistry (A. Padwa, Ed.), Vol. 1, p. 1. Wiley, New York 1984.
3a. Hawker C. J., Wooley K. L.: Science 2005, 309, 1200. <https://doi.org/10.1126/science.1109778>
3b. Binder W. H., Kluger C.: Curr. Org. Chem. 2006, 10, 1791. <https://doi.org/10.2174/138527206778249838>
3c. Lutz J.-F.: Angew. Chem., Int. Ed. 2007, 46, 1018. <https://doi.org/10.1002/anie.200604050>
4. Girard C., Onen E., Aufort M., Beauviere S., Samson E., Herscovici J.: Org. Lett. 2006, 8, 1689. <https://doi.org/10.1021/ol060283l>
5. Lipshutz B. H., Taft B. R.: Angew. Chem., Int. Ed. 2006, 118, 8415. <https://doi.org/10.1002/ange.200603726>
6. Appukkuttan P., Dehaen W., Gokin V., Van der Eycken E.: Org. Lett. 2004, 6, 4223. <https://doi.org/10.1021/ol048341v>
7. Barge A., Cravotto G., Robaldo B., Gianolio E., Aime S.: J. Inclusion Phenom., Macrocycl. Chem. 2007, 57, 489. <https://doi.org/10.1007/s10847-006-9239-2>
8. Rostovtsev V. V., Green G. L., Fokin V. V., Sharpless K. B.: Angew. Chem., Int. Ed. 2002, 41, 2596. <https://doi.org/10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4>
9a. Levêque J.-M., Cravotto G.: Chimia 2006, 60, 313. <https://doi.org/10.2533/000942906777836255>
9b. Cravotto G., Cintas P.: Chem. Eur. J. 2007, 13, 1902. <https://doi.org/10.1002/chem.200601845>
10. Buffa C., Cravotto G., Omiccioli G.: Patent application filed.
11. Hoogenboom R., Moore B., Schubert U.: Chem. Commun. 2006, 4010. <https://doi.org/10.1039/b608313g>
12. Trotta F., Martina K., Robaldo B., Barge A., Cravotto G.: J. Inclusion Phenom., Macrocycl. Chem. 2007, 57, 3. <https://doi.org/10.1007/s10847-006-9169-z>
13. Cravotto G., Omiccioli G., Stevanato L.: Ultrason. Sonochem. 2005, 12, 213. <https://doi.org/10.1016/j.ultsonch.2004.01.002>
14. Aime S., Gianolio E., Robaldo B., Barge A., Cravotto G.: Org. Biomol. Chem. 2006, 4, 1124. <https://doi.org/10.1039/b517068k>