References
- Lee, C. K.; Lee, I.-S. H. Bull. Korean Chem. Soc. 2008, 29, 2205-2208. https://doi.org/10.5012/bkcs.2008.29.11.2205
- Jeon, K. O.; Yu, J. S.; Lee, C. K. Heterocycles 2007, 71, 153-164. https://doi.org/10.3987/COM-06-10925
- Jeon, K. O.; Yu, J. S.; Lee, C. K. J. Heterocyclic Chem, 2003, 40, 763-771. https://doi.org/10.1002/jhet.5570400504
- Jeon, K. O.; Yu, J. S.; Lee, C. K. Bull. Korean Chem. Soc. 2002, 23, 1241-1246. https://doi.org/10.5012/bkcs.2002.23.9.1241
- Lee, C. K.; Yu, J.S.; Lee, H.-J. J. Heterocyclic Chem. 2002, 39, 1207-1217. https://doi.org/10.1002/jhet.5570390615
- Lee, C. K.; Yu, J. S.; Ji, Y. R. J. Heterocyclic Chem. 2002, 39, 1219-1227. https://doi.org/10.1002/jhet.5570390616
- Akalay, D.; Duerner, G.; Goebel, M. W. Eur. J. Org. Chem. 2008, 2365-2368.
- Hoshino, M.; Matsuzaki, H.; Fujita, R. Chem. Pharm. Bull. 2008, 56, 480-484. https://doi.org/10.1248/cpb.56.480
- Brummond, K. M.; Chen, D.; Painter, T. O.; Mao, S.; Seifried, D. D. Synlett 2008, 759-764.
- Al-Mousawi, S. M.; EL-Apasery, M. A.; Elnagdi, M. H. Heterocycles 2008, 75, 1151-1161. https://doi.org/10.3987/COM-07-11301
- Metwally, N. H. Heterocycles 2008, 75, 319-329. https://doi.org/10.3987/COM-07-11208
- Yu, H.; Lee, P. H. J. Org. Chem. 2008, 73, 5183-5186 https://doi.org/10.1021/jo800594y
- Chou, S.-S. P.; Wang, H.-C.; Chen, P.-W.; Yang, C.-H. Tetrahedron 2008, 64, 5291-5297. https://doi.org/10.1016/j.tet.2008.03.030
- Bojase, G.; Payne, A. D.; Willis, A. C.; Sherburn, M. S. Angew. Chem. Int. Ed. 2008, 47, 910-912. https://doi.org/10.1002/anie.200704470
- Kluger, R.; Hunt, J. C. J. Am. Chem. Soc. 1989, 111, 5921-5925. https://doi.org/10.1021/ja00197a062
- Martin, S. F.; Limberakis, C. Tetrahedron Lett. 1997, 38, 2617-2620. https://doi.org/10.1016/S0040-4039(97)00443-7
- Le, Z.-G.; Chen, Z.-C.; Hu, Y.; Zheng, Q.-G. Synthesis 2004, 995-998.
- Lan, J.-B.; Zhang, G.-L.; Yu, X.-Q.; You, J.-S.; Chen, L.; Yan, M.; Xie, R.-G. Synlett 2004, 1095-1097.
- Pal, B.; Pradhan, P. K.; Jaisankar, P.; Giri, V. S. Synthesis 2003, 1549-1552.
- Kar, A.; Argade, N. P. Synthesis 2002, 221-224.
- Cava, M. P.; Deana, A. A.; Muth, K.; Mitchell, M. J. Org. Syn. Col. Vol. V 1973, 944-946.
- Kishikawa, K.; Naruse, M.; Kohmoto, S.; Yamamoto, M.; Yamaguchi, K. J. Chem. Soc. Perkin Trans. 1 2001, 462-468.
- Keana, J. F. W.; Ogan, M. D.; Lu, Y.; Beer, M.; Varkey, J. J. Am. Chem. Soc. 1986, 108, 7957-7963. https://doi.org/10.1021/ja00285a013
- Mederski, W. W. K. R.; Baumgarth, M.; Germann, M.; Kux, D.; Weitzel, T. Tetrahedron Lett. 2003, 44, 2133-2136. https://doi.org/10.1016/S0040-4039(03)00167-9
- Lee, H. S.; Yu, J. S.; Lee, C. K. Magn. Reson. Chem. 2009, 47, 711-715. https://doi.org/10.1002/mrc.2450
- Kalinowski, H.-O.; Berger, S.; Braun, S. Carbon-13 NMR Spectroscopy; John Wiley & Sons: New York, 1984; pp 311-325.
- Craik, D. J.; Brwonlee, R. T. C. Prog. Phys. Org. Chem. 1983, 14, Chapter 1.
-
$\sigma$ values are taken from reference 6, p 321 - Yuzuri, T.; Suezawa, H.; Hirota, M. Bull. Chem. Soc. Jpn. 1994, 67, 1664-1673. https://doi.org/10.1246/bcsj.67.1664
-
Cis-coupling constant ranges 6 to 15 Hz: Pavia, D. L.; Lampman, G. M.; Kriz, G. S.; Vyvyan, J. R. Introduction to Spectroscopy,
$4^{th}^$ Ed.; Brooks/Cole: Belmont, CA, 2009; p 140.
Cited by
- Synthesis of 1-(4-((E)-3-arylacryloyl) phenyl)-3,4-dibromo-1H-pyrrole-2,5-diones and screening for anti-Candida and antituberculosis activity vol.21, pp.8, 2012, https://doi.org/10.1007/s00044-011-9718-x
- Silica sulfuric acid-catalyzed Claisen-Schmidt condensation of 1,3,4 trisubstituted pyrrole 2,5 dione to chalcones vol.38, pp.9, 2012, https://doi.org/10.1007/s11164-012-0553-6
- Se NMR Spectroscopy As a Sensitive Probe for Hammett σ Constants vol.80, pp.8, 2015, https://doi.org/10.1021/acs.joc.5b00108