References
- Haslam, E. Tetrahedron 1980, 36, 2409-2433. https://doi.org/10.1016/0040-4020(80)80219-5
- Gimenez, J.; Costa, J.; Cervera, S. Ind. Eng. Chem. 1987, 26, 198-202. https://doi.org/10.1021/ie00062a004
- Zhang, H. B.; Zhang, B. Z.; Li, H. X. J. Nat. Gas. Chem. 1992, 1, 49-56.
- Corma, A.; Garcia, H.; Iborra, S.; Primo, J. J. Catal. 1989, 120, 78-87. https://doi.org/10.1016/0021-9517(89)90252-2
- Chen, Z. H.; Lizuka, T.; Tanabe, K. Chem. Lett. 1984, 1085.
- Hino, M.; Arata, K. Chem. Lett. 1981, 167.
- Verhoef, J. M.; Kooyan, J. P.; Peters, A. J.; van Bekkum, H. Micropor. Mesopor. Mater. 1999, 27, 365-371. https://doi.org/10.1016/S1387-1811(98)00269-8
- Chu, W.; Yang, X.; Ye, X. K.; Wu, Y. Appl. Catal. A: Gen. 1996, 145, 125-140. https://doi.org/10.1016/0926-860X(96)00109-3
- Li, Y. O. Petrochem.Technol. 1981, 54, 309 (in Chinese).
- Campelo, J. M.; Climent, M. S.; Marinas, J. M. Appl. Catal. 1982, 3, 315-325. https://doi.org/10.1016/0166-9834(82)80266-2
- Bezouhonova, C.; Al-Zihari, M. A. Appl. Catal. A: Gen. 1992, 83, 45-49. https://doi.org/10.1016/0926-860X(92)80024-7
- Sato, S.; Koizumi, K.; Nozaki, F. J. Catal. 1998, 178, 264-274. https://doi.org/10.1006/jcat.1998.2159
- VenkatRao, V.; Chary, K. V. R.; Durgakumari, V.; Narayanan, S. Appl. Catal. 1990, 61, 89-97. https://doi.org/10.1016/S0166-9834(00)82137-5
- Beltrame, P.; Beltrame, P. L.; Carniti, P.; Castelli, A.; Forni, L. Appl. Catal. 1987, 29, 327-334. https://doi.org/10.1016/S0166-9834(00)82902-4
- Adeeva, V.; Dettaan, J. W.; Janchen, J.; Lei, G. D.; Scheunemann, V.; van de Van, L. J. M.; Sachtler, W. M. H.; van Santen, R. A. J. Catal. 1995, 151, 364-372. https://doi.org/10.1006/jcat.1995.1039
- Lin, C. H.; Hsu, C. Y. J. Chem. Soc. Chem. Commun. 1992, 1479-1480.
- Adeeva, V.; Lei, G. D.; Sachtler, W. M. H. Appl. Catal. A: Gen. 1994, 118, L11-L15. https://doi.org/10.1016/0926-860X(94)80084-7
- Mercera, P. D. L.; van Ommen, J. G.; Doesburg, E. B. M.; Burggraaf, A. J.; Ross, J. R. H. Appl. Catal. 1991, 71, 363-391. https://doi.org/10.1016/0166-9834(91)85092-A
- Lahousse, C.; Aboulayt, A.; Mauge, F.; Bachelier, J.; Lavalley, J. C. J. Mol. Catal. 1993, 84, 283-297. https://doi.org/10.1016/0304-5102(93)85061-W
- Ghiaci, M.; Abbaspur, A.; Kalbasi, R. J. Appl. Catal. A: Gen. 2005, 287, 83-88. https://doi.org/10.1016/j.apcata.2005.03.045
- Ghiaci, M.; Kalbasi, R. J.; Mollahasani, M.; Aghaei, H. Appl. Catal. A: Gen. 2007, 320, 35. https://doi.org/10.1016/j.apcata.2006.12.013
- Ghiaci, M.; Kalbasi, R. J.; Aghaei, H. Catal. Commun. 2007, 8, 1843. https://doi.org/10.1016/j.catcom.2007.02.026
- Maki, T.; Ishihara, K.; Yamamoto, H. Org. Lett. 2005, 7, 5047-5050. https://doi.org/10.1021/ol052061d
- Green, I. R.; Tocoli, F. E.; Lee, S. H.; Nihei, K. I.; Kubo, I. European Journal of Medicinal Chemistry 2008, 43, 1315-1320. https://doi.org/10.1016/j.ejmech.2007.08.012
- Timmermans, J. Bulletin des Societes Chimiques Belges 1927, 36, 502-518.
- Qin, G-p. Tianranqi Huagong 2004, 29, 68-71.
- Liu, Z. Huazhong Shifan Daxue Xuebao, Ziran Kexueban 1987, 21, 360-366.
- Shekarriz, M.; Taghipoor, S.; Khalili, A. A.; Jamarani, M. S. Journal of Chemical Research, Synopses 2003, 172-173.
- Kudo, T.; Nose, A. Yakugaku Zasshi 1975, 95, 1411-1417. https://doi.org/10.1248/yakushi1947.95.12_1411
- Won, J. E.; Kim, H. K.; Kim, J. J.; Yim, H. S.; Kim, M. J.; Kang, S. B.; Chung, H. A.; Yoon, Y. J. Tetrahedron 2007, 63, 12720-12730. https://doi.org/10.1016/j.tet.2007.10.011
- Huang, H. Jilin Daxue Ziran Kexue Xuebao 1987, 4, 71-75.
- McNulty, J.; Nair, J. J.; Robertson, Al. J. Org. Lett. 2007, 9, 4575-4578. https://doi.org/10.1021/ol702081g
- McNulty, J.; Nair, J. J; Cheekoori, S.; Larichev, V.; Capretta, A.; Robertson, Al. J. Chemistry-A European Journal 2006, 12, 9314-9322. https://doi.org/10.1002/chem.200600653
- Talvitie, Y. Ann. Acad. Sci. Fennicae 1927, 26A, 1-94.
- Behloul, C.; Guijarro, D.; Yus, M. Synthesis 2006, 2, 309-314.
- Aimo, G. Synthesis 1979, 3, 223-227.
- Barluenga, J. Synthesis 1983, 8, 649-51.
- Barrett, A. G. M.; Werner, T. J. Org. Chem. 2006, 71(11), 4302-4304. https://doi.org/10.1021/jo060562m
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