Baozhi Li

Jing Kang

Qiang Gu

Shuaijun Wang

Tianqi Zhao

Yuanhui He

Yumin Zhang

Comptes Rendus Chimie

Supporting informationFacile synthesis of trisubstituted imidazoles from 1,2-di(furan-2-yl)-2-oxoethyl carboxylates and their chemiluminescenceBaozhi Li, Qiang Gu, Yuanhui He, Tianqi Zhao, Xiaodong Chen, Shuaijun Wang, Jing Kang, Yumin Zhang*College of Chemistry, Jilin University, Changchun 130012, P. R. China*Corresponding Author: Professor Yumin Zhang. Tel: (+86)-431-85168470 (3). 1H NMR and 13C NMR spectra of the synthesized compounds1. 1H NMR and 13C NMR for 4,5-di(furan-2-yl)-2-phenyl-1H-imidazole (3a) (Table 3, entry 1)1H NMR of 4,5-di(furan-2-yl)-2-phenyl-1H-imidazole13C NMR of 4,5-di(furan-2-yl)-2-phenyl-1H-imidazole2. 1H NMR and 13C NMR for 4,5-di(furan-2-yl)-2-(4-methylphenyl)-1H- imidazole (3b) (Table 3, entry 2)1H NMR of 4,5-di(furan-2-yl)-2-(4-methylphenyl)-1H-imidazole13C NMR of 4,5-di(furan-2-yl)-2-(4-methylphenyl)-1H-imidazole3. 1H NMR and 13C NMR for 4,5-di(furan-2-yl)-2-(4-chlorophenyl)-1H-imidazole (3c) (Table 3, entry 3)1H NMR of 4,5-di(furan-2-yl)-2-(4-chlorophenyl)-1H-imidazole13C NMR of 4,5-di(furan-2-yl)-2-(4-chlorophenyl)-1H-imidazole4. 1H NMR and 13C NMR for 4,5-di(furan-2-yl)-2-(2-furylvinyl)-1H-imidazole (3d) (Table 3, entry 4)1H NMR of 4,5-di(furan-2-yl)-2-(2-furylvinyl)-1H-imidazole13C NMR of 4,5-di(furan-2-yl)-2-(2-furylvinyl)-1H-imidazole5. 1H NMR and 13C NMR for 4,5-di(furan-2-yl)-2-(1-chloro-2,2-dimethylethyl)- 1H-imidazole (3e) (Table 3, entry 5)1H NMR of 4,5-di(furan-2-yl)-2-(1-chloro-2,2-dimethylethyl)-1H-imidazole13C NMR of 4,5-di(furan-2-yl)-2-(1-chloro-2,2-dimethylethyl)- 1H-imidazole6. 1H NMR and 13C NMR for 4,5-di(furan-2-yl)-2-methyl-1H-imidazole (3f) (Table 3, entry 6)1H NMR of 4,5-di(furan-2-yl)-2-methyl-1H-imidazole13C NMR of 4,5-di(furan-2-yl)-2-methyl-1H-imidazole7. 1H NMR and 13C NMR for 4,5-di(furan-2-yl)-2-(4-nitrophenyl)-1H-imidazole (3g) (Table 3, entry 7)1H NMR of 4,5-di(furan-2-yl)-2-(4-nitrophenyl)-1H-imidazole13C NMR of 4,5-di(furan-2-yl)-2-(4-nitrophenyl)-1H-imidazole8. 1H NMR and 13C NMR for 3-(4,5-di(furan-2-yl)-1H-imidazol-2-yl)pyridine (3h) (Table 3, entry 8)1H NMR of 3-(4,5-di(furan-2-yl)-1H-imidazol-2-yl)pyridine13C NMR of 3-(4,5-di(furan-2-yl)-1H-imidazol-2-yl)pyridine9. 1H NMR and 13C NMR for 4,5-di(furan-2-yl)-2-undecyl-1H-imidazole (3i) (Table 3, entry 9)1H NMR of 4,5-di(furan-2-yl)-2-undecyl-1H-imidazole13C NMR of 4,5-di(furan-2-yl)-2-undecyl-1H-imidazole10. 1H NMR and 13C NMR for 2,4,5-tri(furan-2-yl)-1H-imidazole (3j) (Table 3, entry 10)1H NMR of 2,4,5-tri(furan-2-yl)-1H-imidazole13C NMR of 2,4,5-tri(furan-2-yl)-1H-imidazole11. 1H NMR and 13C NMR for 4,5-di(furan-2-yl)-2-styryl-1H-imidazole (3k) (Table 3, entry 11)1H NMR of 4,5-di(furan-2-yl)-2-styryl-1H-imidazole13C NMR of 4,5-di(furan-2-yl)-2-styryl-1H-imidazolePAGE  S12

Facile synthesis of trisubstituted imidazoles from 1,2-di(furan-2-yl)-2-oxoethyl carboxylates and their chemiluminescence

https://comptes-rendus.academie-sciences.fr/chimie/article/10.1016/j.crci.2012.06.005/file/attach/mmc1.doc

Facile synthesis of trisubstituted imidazoles from 1,2-di(furan-2-yl)-2-oxoethyl carboxylates and their chemiluminescence

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