References
- Morton, F. A.; Linduska, J. P. J. Econ. Entomol. 1947, 40, 562-564. https://doi.org/10.1093/jee/40.4.562
- Travis, B. V.; Morton, F. A.; Jones, H. A.; Robinson, J. H.J. Econ. Entomol. 1949, 42, 686-694. https://doi.org/10.1093/jee/42.4.686
- Smith, C. N.; Burnett, D. J. Econ. Entomol 1949, 42, 439-444. https://doi.org/10.1093/jee/42.3.439
- Piper, Hall, Wright, Ind. Eng. Chem. 1951, 43, 11a. https://doi.org/10.1021/ie50502a001
- Barthel, W. F.; Leon, J.; Hall, S. A. J. Org. Chem. 1954, 19, 485-489. https://doi.org/10.1021/jo01369a001
- Cohen, S. G.; Schultz, R. M.; Weinstein, S. Y. J. Am. Chem. Soc. 1966, 88, 5315-5319. https://doi.org/10.1021/ja00974a052
- Elsenbaumer, R. L.; Mosher, H. S. J. Org. Chem. 1979, 44(4),600-604. https://doi.org/10.1021/jo01318a024
- Huszthy, P.; Bradshaw, J. S.; Zhu, C. Y.; Izatt, R. M. J. Org. Chem. 1991, 56, 3330-3336. https://doi.org/10.1021/jo00010a028
- Zhang, G. S.; Gong, H. Synth. Commun. 1999, 29(9), 1547-1551. https://doi.org/10.1080/00397919908086134
- Kolasa, T.; Miller, M. J. J. Org. Chem. Rev. 1987, 52, 4978-4984. https://doi.org/10.1021/jo00231a026
- Jin, T. S.; Ma, R. Y.; Li, Y.; Sun, X.; Li, T. S. Synth. Commun. 2001, 31(13), 2051-2054. https://doi.org/10.1081/SCC-100104424
- Mizuno, N.; Misono, M. Chem. Rev. 1998, 98, 199-218. https://doi.org/10.1021/cr960401q
- Okuhara, T.; Mizuno, N.; Misono, M. Adv. Catal. 1996, 41, 113-252. https://doi.org/10.1016/S0360-0564(08)60041-3
- Misono, M. Catal. Rev. Sci. Eng. 1987, 29, 269-321. https://doi.org/10.1080/01614948708078072
- Habibi, M. H.; Tangestaninejad, S.; Mohammadpoor-Baltork, I.; Mirkhani, V.; Yadollahi, B. Tetrahedron Lett. 2001, 42, 2851-2853. https://doi.org/10.1016/S0040-4039(01)00298-2
- Habibi, M. H.; Tangestaninejad, S.; Mirkhani, V.; Yadollahi, B. Tetrahedron 2001, 57, 8333-8337. https://doi.org/10.1016/S0040-4020(01)00806-7
- Habibi, M. H.; Tangestaninejad, S.; Mirkhani, V.; Yadollahi, B. Catalysis Lett. 2001, 75, 205-207. https://doi.org/10.1023/A:1016752307623
- Habibi, M. H.; Tangestaninejad, S.; Mohammadpoor-Baltork, I.; Mirkhani, V.; Yadollahi, B. Tetrahedron Lett. 2001, 42, 6771-6774. https://doi.org/10.1016/S0040-4039(01)01379-X
- Buckingham J.; Donaghy S. M. Heiborn's Dictionary of Organic Compounds, 5th Ed.; New York, 1982.
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