Collect. Czech. Chem. Commun.
2010, 75, 871-885
https://doi.org/10.1135/cccc2010012
Published online 2010-08-20 09:52:04
Synthesis and selected transformations of 3-oxido-1H-imidazole-4-carboxamides
Grzegorz Mloston and Marcin Jasiński*
Department of Organic and Applied Chemistry, University of Łódź, Tamka 12, PL-91-403 Łódź, Poland
References
1a. R., Hahn W., Mlostoń G.: Roczniki Chem. 1977, 51, 49.
1b. I. J., Schofield K.: J. Chem. Soc., Perkin Trans. 1 1975, 275.
<https://doi.org/10.1039/p19750000275>
1c. J., Begtrup M., de la Hoz A.: J. Chem. Soc., Perkin Trans. 1 1995, 2467.
<https://doi.org/10.1039/p19950002467>
1d. H., Gerpe A., Gonzáles M., Fernández Sainz Y., Piro O. E., Castellano E. E.: Synthesis 2004, 2678.
<https://doi.org/10.1055/s-2004-831212>
2a. S., Wagner G., Kotschenreuther D.: Angew. Chem., Int. Ed. 2002, 41, 2290.
<https://doi.org/10.1002/1521-3773(20020703)41:13<2290::AID-ANIE2290>3.0.CO;2-R>
2b. G., Boiani M., Cerecetto H., Gerpe A., González M., Sainz Y. F., Denicola A., de Ocáriz C. O., Nogal J. J., Montero D., Escario J. A.: Arch. Pharm. Pharm. Med. Chem. 2004, 337, 259.
<https://doi.org/10.1002/ardp.200300840>
2c. L.-C., Stuart D. R., Leclerc J.-P., Bertrand-Laperle M., Villemure E., Sun H.-Y., Lasserre S., Guimond N., Lecavallier M., Fagnou K.: J. Am. Chem. Soc. 2009, 131, 3291.
<https://doi.org/10.1021/ja808332k>
2d. Mlostoń G., Jasiński M., Heimgartner H.: J. Heterocycl. Chem. 2010, 47, in press.
3a. G., Gendek T., Heimgartner H.: Helv. Chim. Acta 1998, 81, 1585.
<https://doi.org/10.1002/(SICI)1522-2675(19980909)81:9<1585::AID-HLCA1585>3.0.CO;2-N>
3b. G., Gendek T., Heimgartner H.: Tetrahedron 2000, 56, 5405.
<https://doi.org/10.1016/S0040-4020(00)00449-X>
3c. G., Jasiński M., Linden A., Heimgartner H.: Helv. Chim. Acta 2006, 89, 1304.
<https://doi.org/10.1002/hlca.200690129>
4a. G., Celeda M., Prakash G. K. S., Olah G. A., Heimgartner H.: Helv. Chim. Acta 2000, 83, 728.
<https://doi.org/10.1002/(SICI)1522-2675(20000412)83:4<728::AID-HLCA728>3.0.CO;2-B>
4b. Jasiński M.: Ph.D. Thesis. University of Łódź, Łódź 2008.
5. H.: Z. Chem. 1970, 10, 462.
<https://doi.org/10.1002/zfch.19700101206>
6. R., Lettau H., Nuhn P., Schneider R., Stenger P., Stiebitz B.: Pharmazie 1991, 46, 412.
7. M., Mlostoń G., Linden A., Heimgartner H.: Helv. Chim. Acta 2008, 91, 1916.
<https://doi.org/10.1002/hlca.200890205>
8. P., Mlostoń G., Jasiński M., Linden A., Heimgartner H.: Tetrahedron: Asymmetry 2008, 19, 1600.
<https://doi.org/10.1016/j.tetasy.2008.06.015>
9. I. R., Jr., Moran P. J. S.: Tetrahedron 1999, 55, 14221.
<https://doi.org/10.1016/S0040-4020(99)00897-2>
10. O. P., Satti N. K., Suri K. A.: Synth. Commun. 2000, 30, 3709.
<https://doi.org/10.1080/00397910008086998>
11a. V. V., Green L. G., 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>
11b. S. K., Reddy M. S., Mangle M., Ganesh K. R.: Tetrahedron 2007, 63, 126.
<https://doi.org/10.1016/j.tet.2006.10.031>
12. L.: Z. Phys. Chem., B 1939, 43, 364.
13. E. V., Davis H. W.: J. Org. Chem. 1967, 32, 1562.
<https://doi.org/10.1021/jo01280a058>
14. I., Perlinger H., Behringer L.: Chem. Ber. 1958, 91, 2330.
<https://doi.org/10.1002/cber.19580911111>
15. T., Tokizawa M., Nohira H., Takei H.: J. Org. Chem. 1961, 26, 4381.
<https://doi.org/10.1021/jo01069a048>
16. E.: Synthesis 1972, 475.
<https://doi.org/10.1055/s-1972-21903>
17. M. R., Mankad B. N.: J. Indian Chem. Soc. 1964, 41, 841.
18. P. W., Burgard A., Thier W.: Justus Liebigs Ann. Chem. 1936, 526, 277.
<https://doi.org/10.1002/jlac.19365260117>

