References
- Green, G. R.; Evans, J. M.; Vong, A. K. In Comprehensive Heterocyclic Chemistry II; Katritzky, A. R.; Ress, C. W.; Scriven, E. F. V., Eds.; Pergamon Press: Oxford, 1995; Vol. 5, p. 469
- (a) Foye, W. O. Principi Di Chemico Farmaceutic Piccin: Padova, Italy, 1991; p. 416 (Please refer to the other references for details:no.11)
- Konkoy, C. S.; Fisck, D. B.; Cai, S. X.; Lan, N. C.; Keana, J. F. W. PCT Int. Appl. WO 0075123, 2000; Chem. Abstr. 2001, 134, 29313a.
- (a) Hall, N. Science 1994, 266, 32. (Please refer to the other references for details:no.12) https://doi.org/10.1126/science.266.5182.32
- (a) Bamoharram, F. F.; Heravi, M. M.; Roshani, M.; Gharib, A.; Jahangir, M. Appl. Catal. 2006, 302, 42 (Please refer to the other references for details:no.13~no.19) https://doi.org/10.1016/j.molcata.2005.12.025
- Elagamay, A. G. A.; El-Taweel, F. M. A. A. Indian J. Chem. B. 1990, 29, 885
- Ballini, R.; Bosica, G.; Conforti, M. L.; Maggi, R.; Mazzacanni, A.; Righi, P.; Sartori, G. Tetrahedron. 2001, 57, 1395 https://doi.org/10.1016/S0040-4020(00)01121-2
- Shi, D. Q.; Zhang, S.; Zhuang, Q. Y.; Tu, S. J.; Hu, H. W. Youji Huaxue. 2003, 23, 809
- Maggi, R.; Ballini, R.; Sartori, G.; Sartorio, R. Tetrahedron Lett. 2004, 45, 2297 https://doi.org/10.1016/j.tetlet.2004.01.115
- Jin, T.-Sh.; Xiao, J.-Ch.; Wang, S.-J.; Li, T.-Sh. Ultrason. Sonochem. 2004, 11, 393 https://doi.org/10.1016/j.ultsonch.2003.10.002
- (b) Witte, E. C.; Neubert. P.; Roesch, A. Ger. Offen DE. Chem. Abstr. 1986, 104, 224915f. (The reference is seperated at no.2)
- (b) Domling, A.; Herdtweck, E.; Ugi. I. Acta.Chem. Scand. 1998, 52, 107. (The reference is seperated at no.4) https://doi.org/10.3891/acta.chem.scand.52-0107
- (b) Heravi, M. M.; Hekmatshoar, R.; Pedram, L. J. Mol. Catal. A: Chem. 2005, 89, 231 (The reference is seperated at no.5) https://doi.org/10.1016/j.molcata.2005.01.005
- (c) Tajbakhsh, M.; Mohajerani, B.; Heravi, M. M.; Ahmadi, A. N. J. Mol. Catal. A: Chem. 2005, 236, 216 (The reference is seperated at no.5) https://doi.org/10.1016/j.molcata.2005.04.033
- (d) Bigdeli, M. M.; Nahid, M. A.; Ajami, D. Indian J. Chem. B. 1999, 38, 1285 (The reference is seperated at no.5)
- (e) Heravi, M. M.; K. Bakhtiari, K.; Bamoharram, F. F. Catal. Commun. 2006, 7, 373 (The reference is seperated at no.5) https://doi.org/10.1016/j.catcom.2005.12.007
- (f) Bamoharram, F. F.; Heravi, M. M.; Roshani, M.; Gharib, A.; Jahangir, M. J. Mol. Catal. A: Chem. 2006, 252, 90 (The reference is seperated at no.5) https://doi.org/10.1016/j.molcata.2006.01.067
- (g) Bamoharram, F. F.; Heravi, M. M.; Roshani, M.; Tavakoli, N. J. Mol. Catal. A: Chem. 2006, 252, 219 (The reference is seperated at no.5) https://doi.org/10.1016/j.molcata.2006.02.059
- (h) Tajbakhsh, M.; Heravi, M. M.; Mohajerani, B.; Ahmadi, A. N. J. Mol. Catal. A: Chem. 2005, 236, 213 (The reference is seperated at no.5) https://doi.org/10.1016/j.molcata.2005.04.033
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