References
- Knoevenagel, E. Chem. Ber. 1984, 27, 2345.
- Trost, B. M. Comprehensive Organic Synthesis; Pergamon Press: Oxford, 1991; vol. 2, p 133.
- Freeman, F. Chem. Rev. 1981, 80, 329. https://doi.org/10.1021/cr60326a004
- Tietze, L. F.; Saling, P. Synlett 1992, 281.
- Borah, H. N.; Deb, M. L.; Boruah R. C.; Bhuyan, P. J. Tetrahedron Lett. 2005, 46, 3391. https://doi.org/10.1016/j.tetlet.2005.03.091
- Tietze, L. F. Chem. Rev. 1996, 96, 115. https://doi.org/10.1021/cr950027e
- Fatiadi, A. J. Synthesis 1978, 165 and 241; and references cited therein.
- Japan Pharmaceutical References, First ed.; 1989-90; p 144.
- Abbott, T.; Johnson, J. Organic Synthesis Coll.; John Wiley and Sons: New York, 1941; Vol. I, p 440.
- Rong, L.; Li, X.; H, Li.; Wang, D. S.; Tu, S.; Zhuang, Q. Synth. Commun. 2006, 36, 2407. https://doi.org/10.1080/00397910600640289
- Dave, C. G.; Augustine, C. Indian J. Chem. 2000, 39B, 403.
- Liu, X.-W.; Jiang, H.; Gong, H. Chinese J. Org. Chem. 2007, 27, 131
- Abaee, M. S.; Mojtahedi, M. M.; Zahedi, M. M.; Khanalizadeh, G. Arkivoc 2006, xv, 48.
- Balalaie, S.; Nemati, N. Synth. Commun. 2000, 30, 869. https://doi.org/10.1080/00397910008087099
- Loupy, A.; Song, S. J.; Sohn, S. M.; Lee, Y. M.; Kon, T. W. J. Chem. Soc. Perkin Trans. 1 2001, 1220.
- Bandgar, B. P.; Uppalla, L. S.; Sadavarte, V. S. J. Res (S) 2002, 40.
- Kidwai, M.; Sapra, P.; Bhushan, K. R. J. Indian Chem. Soc. 2002, 79, 596.
- Shi, D. Q.; Wang, X. S.; Yao, C. S.; Mu, L. J. Chem. Res (S) 2002, 344.
- Bigi, F.; Conforti, M. L.; Maggi, R.; Piccinno, A.; Sartoni, G. Green Chem. 2000, 2, 101. https://doi.org/10.1039/b001246g
- Sebti, S.; Nazith, R.; Tahir, R.; Saber, A. Synth. Commun. 2001, 31, 993. https://doi.org/10.1081/SCC-100103527
- Peng, Y.; Song, G. Indian J. Chem. 2003, 42B, 924.
- Zuo, W. Z.; Hua, R.; Qiu, X. Synth. Commun. 2004, 34, 3219. https://doi.org/10.1081/SCC-200028628
- Reddy, K. R.; Rajgopal, K.; Maheshwari, C. U.; Lakshmikantam, M. New J. Chem. 2006, 30, 1549. https://doi.org/10.1039/b610355c
- Khan, F. A.; Dash, J.; Satapathy, R.; Upadhay, S. K. Tetrahedron Lett. 2004, 45, 3055. https://doi.org/10.1016/j.tetlet.2004.02.103
- Zhng, X.; Lai, E. M.; Aranda, R. M.; Yeung, K. L. Appl. Catal. A: Gen. 2004, 261, 109. https://doi.org/10.1016/j.apcata.2003.10.045
- Tamami, B.; Fadavi, A. Iranian Poly. J. 2006, 15, 331.
- Sebti, S.; Smahi, A.; Solhy, A. Tetrahedron Lett. 2002, 43, 1813. https://doi.org/10.1016/S0040-4039(02)00092-8
- Jin, T. S.; Zhang, J.-S.; Wang, A.-Q.; Li, T.-S. Synth. Commun. 2004, 34, 2611 https://doi.org/10.1081/SCC-200025621
- Oskooie, H. A.; Heravi, M. M.; Derikvand, F.; Khorasani, M. Synth. Commun. 2006, 36, 2819. https://doi.org/10.1080/00397910600770631
- Boullet, F. T.; Foucaud, A. Tetrahedron Lett. 1982, 23, 4927. https://doi.org/10.1016/S0040-4039(00)85749-4
- Li, Y.-Q.; Ye, H.-H. Chin. J. Org. Chem. 2002, 22, 678.
- Moal, H.; Carrie, R.; Focuad, A.; Bargain, M.; Sevellec, C. Bull. Soc. Chim. Fr. 1966, 1033.
- Carrie, B. Bull. Soc. Sci.1962, 37, 5.
- Nagaei, M.; Zasshi, N. K. 1968, 89, 958; Chem. Abstr. 1970, 67824.
- Jones, R. A. Y. J. Chem. Soc. Perkin Trans. 1972, 2, 34.
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