Pure Appl. Chem., 2011, Vol. 83, No. 3, pp. 709-713
http://dx.doi.org/10.1351/PAC-CON-10-09-29
Published online 2011-01-27
Efficient and green synthesis of new polycyclic procyanidin derivatives via tandem dinucleophilic addition of indolin-2-thiones to flavylium salts
References
- 1a. H. Arch. Biochem. Biophys. 459, 214 (2007). ( , M. M. Polansky, R. A. Anderson. http://dx.doi.org/10.1016/j.abb.2006.12.034)
- 1b. D.‑Y. Phytochemistry 66, 2127 (2005). ( , R. A. Dixon. http://dx.doi.org/10.1016/j.phytochem.2005.01.008)
- 1c. R. A. J. Agric. Food Chem. 52, 65 (2004). ( , C. L. Broadhurst, M. M. Polansky, W. F. Schmidt, A. Khan, V. P. Flanagan, N. W. Schoene, D. J. Graves. http://dx.doi.org/10.1021/jf034916b)
- 1d. D. A. Nat. Prod. Rep. 18, 583 (2001). .
- 1e. O. J. Chem. Soc., Perkin Trans 2 1653 (2000). ( , G. Fargeix, C. Dufour. http://dx.doi.org/10.1039/b003260n)
- 1f. J. Horm. Res. 50, 177 (1998). ( , S. Deas, M. M. Polansky, D. A. Baedke, T. S. Ingebritsen, R. A. Anderson, D. J. Graves. http://dx.doi.org/10.1159/000023270)
- 2a. S. K. J. Cell Biochem. 67, 59 (1997). ( , H. Mukhtar. http://dx.doi.org/10.1002/(SICI)1097-4644(1997)27+<59::AID-JCB11>3.0.CO;2-G)
- 2b. M. J. Agric. Food Chem. 47 (1999). , M. Suzuki, T. Miyase, K. Yoshino, M. Maeda-Yamamoto.
- 2c. S. Bioorg. Med. Chem. 11, 3371 (2003). ( , S. T. Tian, H. Wang, R. E. Stark, R. T. Rosen. http://dx.doi.org/10.1016/S0968-0896(03)00367-5)
- 2d. A. Phytochemistry 30, 3875 (1991). ( . http://dx.doi.org/10.1016/0031-9422(91)83426-L)
- 2e. T. Food Chem. Toxicol. 37, 545 (1999). , Y. Yokoo, T. Inoue, A. Ishii.
- 3a. T. Bioorg. Med. Chem. Lett. 8, 1801 (1998). ( , R. Kusano, I. Kouno. http://dx.doi.org/10.1016/S0960-894X(98)00311-4)
- 3b. J. L. J. Agric. Food Chem. 49, 4627 (2001). ( , R. Bobet. http://dx.doi.org/10.1021/jf010368v)
- 3c. H. J. Agric. Food Chem. 55, 1525 (2007). ( , T. Nakagawa, H. Nishioka, E. Sato, A. Hirose, Y. Ueno, B. Sun, T. Yokozawa, G. I. Nonaka. http://dx.doi.org/10.1021/jf062819n)
- 3d. J. L. Bioorg. Med. Chem. 10, 2497 (2002). ( , C. Lozano, L. Julia, F. J. Sanchez-Baeza, J. M. Anglada, J. J. Centelles, M. Cascante. http://dx.doi.org/10.1016/S0968-0896(02)00127-X)
- 4a. G. A. Molecules 14, 807 (2009). ( , Y. Yuan, A. Kempema. http://dx.doi.org/10.3390/molecules14020807)
- 4b. F. Molecules 13, 3007 (2008). ( , Q. H. Pan, Y. Shi, C. Q. Duan. http://dx.doi.org/10.3390/molecules13123007)
- 4c. G. A. Kraus, Y. Yuan. U.S. Pat. Appl. Publ., 17. CODEN: USXXCO US 2007173543 A1 20070726 (2007).
- 4d. A. M. Tetrahedron Lett. 48, 1163 (2007). ( , K. K. Y. Wong. http://dx.doi.org/10.1016/j.tetlet.2006.12.075)
- 4e. C. Tetrahedron 62, 5298 (2006). ( , T. R. R. Pettus. http://dx.doi.org/10.1016/j.tet.2006.01.109)
- 4f. K. Tetrahedron Lett. 41, 485 (2000). ( , M. Kurihara, K. Fukuhara, T. Tanaka, T. Suzuki, N. Miyata. http://dx.doi.org/10.1016/S0040-4039(99)02097-3)
- 4g. S. Chem. Pharm. Bull. 35, 4717 (1987). , G. Nonaka, I. Nishioka.
- 4h. A. Liebigs. Ann. Chem. 597 (1977). .
- 5a. J. L. Org. Lett. 10, 4823 (2008). ( , J. B. Wong, P. Y. Kuo, D. Y. Yang. http://dx.doi.org/10.1021/ol8018902)
- 5b. G. Trends Food Sci. Tech. 15, 191 (2004). ( , J. M. Cruz, A. Moure, H. Domínguez, J. C. Parajó. http://dx.doi.org/10.1016/j.tifs.2003.09.016)
- 5c. A. J. Am. Chem. Soc. 125, 987 (2003). ( , C. Lodeiro, F. Pina, M. Maestri, S. Dumas, P. Passaniti, V. Balzani. http://dx.doi.org/10.1021/ja0287276)
- 5d. A. Lietti, A. Bonati. U.S. Patent 4258055.
- 5e. Y. Tetrahedron Lett. 42, 1371 (2001). ( , L. Y. Foo. http://dx.doi.org/10.1016/S0040-4039(00)02246-2)
- 5f. A. I. Chem. Heterocycl. Compounds 35, 653 (1999). ( , V. N. Storozhenko, S. G. Storozhenko, A. O. Manyashin, N. T. Berberova, O. Y. Okhlobystin. http://dx.doi.org/10.1007/BF02251620)
- 5g. H. J. Agric. Food Chem. 45, 304 (1997). ( , G. Cao, R. L. Prior. http://dx.doi.org/10.1021/jf960421t)
- 5h. G. A. Tetrahedron 39, 3005 (1983). ( , J. G. Sweeny. http://dx.doi.org/10.1016/S0040-4020(01)91542-X)
- 6a. C. Eur. J. Org. Chem. 4451 (2001). ( , G. Remennikov, H. Mayr. http://dx.doi.org/10.1002/1099-0690(200112)2001:23<4451::AID-EJOC4451>3.0.CO;2-F)
- 6b. C. Czerney, H. Hartmann. In Methoden Org. Chem. (Houben-Weyl), 4th ed., Vol. VII/2Ea, p. 30, R. P. Kreher (Ed.), Thieme Verlag, Stuttgart (1991).
- 6c. G. A. Tetrahedron 39, 3005 (1983). ( , J. G. Sweeny. http://dx.doi.org/10.1016/S0040-4020(01)91542-X)
- 6d. L. J. Heterocycl. Chem. 18, 429 (1981). ( . http://dx.doi.org/10.1002/jhet.5570180244)
- 6e. L. Tetrahedron 23, 1057 (1967). ( . http://dx.doi.org/10.1016/0040-4020(67)85056-7)
- 6f. L. Tetrahedron 21, 3707 (1965). ( . http://dx.doi.org/10.1016/S0040-4020(01)96986-8)
- 7a. A. S. K. Chem. Rev. 107, 3180 (2007). ( . http://dx.doi.org/10.1021/cr000436x)
- 7b. L. F. Tietze, N. Rackelman. In Multicomponent Reactions, J. Zhu, I. Bienayme (Eds.), Wiley-VCH, Weinheim (2005).
- 7c. L. F. Chem. Rev. 96, 115 (1996). ( , http://dx.doi.org/10.1021/cr950027e)
- 7d. K. K. Chem. Rev. 96, 207 (1996). ( . http://dx.doi.org/10.1021/cr950030y)
- 7e. T. L. Ho. Tandem Organic Reactions, John Wiley, New York (1992).
- 8a. F. M. Tetrahedron 66, 134 (2010). ( , Z. Mirjafary, H. Saeidian, S. Taheri, M. Doulabi, M. Kiamehr. http://dx.doi.org/10.1016/j.tet.2009.11.032)
- 8b. F. M. Synlett 123 (2010). ( , S. Taheri, Z. Mirjafary, H. Saeidian. http://dx.doi.org/10.1055/s-0029-1218534)
- 8c. F. M. Tetrahedron Lett. 51, 2704 (2010). ( , Z. Mirjafary, H. Saeidian, S. Taheri, M. R. Khodabakhshi. http://dx.doi.org/10.1016/j.tetlet.2010.03.038)
- 8d. F. M. Tetrahedron 66, 3678 (2010). ( , Z. Mirjafary, H. Saeidian, S. Taheri, B. Soltanzadeh. http://dx.doi.org/10.1016/j.tet.2010.03.078)
- 8e. F. M. Arkivoc xi, 91 (2010). , H. Saeidian, M. Kiamehr, Z. Mirjafary, S. Taheri.