References
- Harborne, J. B.; Williams, C. A. Nat. Prod. Rep. 2001, 18, 310 https://doi.org/10.1039/b006257j
- Tsuchiya, Y.; Shimizu, M.; Hiyama, Y.; Itoh, K.; Hashimoto, Y.; Nakayama, M.; Horie, T.; Morita, N. Chem. Pharm. Bull. 1985, 33, 3881 https://doi.org/10.1248/cpb.33.3881
- Middleton, E.; Kandaswami, C. Food Technol. 1994, 48, 115
- Bors, W.; Michel, C.; Stettmaier, K. BioFactors 1997, 6, 399 https://doi.org/10.1002/biof.5520060405
- Nijveldt, R. J.; Nood, E.; Hoorn, D.; Boelens, P. G.; Norren, K.; Leeuwen, P. Am. J. Clin. Nutr. 2001, 74, 418
- Bohm, B. A. Introduction to Flavonoids; Harwood Academic Publishers: Amsterdam, Netherlands, 1998; p 243
- Wheeler, T. S. Org. Synth. Coll. Vol. 4, 1963, 478
- Nishinaga, A.; Ando, H.; Maruyama, K.; Mashino, T. Synthesis 1992, 839
- Ares, J. J.; Outt, P. E.; Kakodkar, S. V.; Buss, R. C.; Geiger, J. C. J. Org. Chem. 1993, 58, 7903 https://doi.org/10.1021/jo00079a041
- Zembower, D. E.; Zhang, H. J. Org. Chem. 1998, 63, 9300 https://doi.org/10.1021/jo981186b
- Banerji, A.; Goomer, N. C. Synthesis 1980, 874
- Saxena, S.; Makrandi, J. K.; Grover, S. K. Synthesis 1985, 697
- Cushman, M.; Nagarathnam, D. Tetrahedron Lett. 1990, 31, 6497 https://doi.org/10.1016/S0040-4039(00)97100-4
- Nagarathnam, D.; Cushman, M. J. Org. Chem. 1991, 56, 4884 https://doi.org/10.1021/jo00016a015
- Nagarathnam, D.; Cushman, M. Tetrahedron 1991, 47, 5071 https://doi.org/10.1016/S0040-4020(01)87119-2
- Menichincheri, M.; Ballinari, D.; Bargiotti, A.; Bonomini, L.; Ceccarelli, W.; D'Alessio, R.; Fretta, A.; Moll, J.; Polucci, P.; Soncini, C.; Tibolla, M.; Trosset, J. Y.; Vanotti, E. J. Med. Chem. 2004, 47, 6466 https://doi.org/10.1021/jm040810b
- Kasahara, A.; Izumi, T.; Ooshima, M. Bull. Chem. Soc. Jpn. 1974, 47, 2526 https://doi.org/10.1246/bcsj.47.2526
- Ali, S. M.; Iqbal, J.; Ilyas, M. Chem. and Ind. 1985, 276. (c) Makrandi, J. K.; Seema Bull. Chem. Soc. Jpn. 1989, 607
- Hans, N.; Grover, S. K. Synth. Comm. 1993, 23, 1021 https://doi.org/10.1080/00397919308013299
- Litkei, G.; Gulacsi, K.; Antus, S.; Blasko, G. Liebigs Ann. 1995, 1711 https://doi.org/10.1080/00397919308013299
- Miyake, H.; Takizawa, E.; Sasaki, M. Bull. Chem. Soc. Jpn. 2003, 76, 835 https://doi.org/10.1246/bcsj.76.835
- Hercouet, A.; Corre, M. L. Synthesis 1982, 597 https://doi.org/10.1246/bcsj.76.835
- Floch, Y. L.; Lefeuvre, M. Tetrahedron Lett. 1986, 27, 2751 https://doi.org/10.1016/S0040-4039(00)84634-1
- Staunton, J. In Comprehensive Organic Chemistry; Barton, D.; Ollis, W. D., Eds.; Pegamon Press: Oxford, U. K., 1979; Vol. 4, p 679 https://doi.org/10.1016/S0040-4039(00)84634-1
- Blasko, G.; Xun, L.; Cordell, G. A. J. Nat. Prod. 1988, 51, 60 https://doi.org/10.1021/np50055a007
- Lee, J. I.; Son, H. S.; Park, H. Bull. Korean Chem. Soc. 2004, 25, 1945 https://doi.org/10.1021/np50055a007
- Lee, J. I.; Son, H. S.; Park, H. Bull. Korean Chem. Soc. 2004, 25, 1945 https://doi.org/10.5012/bkcs.2004.25.12.1945
Cited by
- Solubility Estimation of High-value Natural Products in Supercritical CO2 Based on Solubility Parameter vol.36, pp.5, 2010, https://doi.org/10.1252/kakoronbunshu.36.466
- An Effective Synthesis of 3-Methoxyflavones via 1-(2-Hydroxyphenyl)-2-methoxy-3-phenyl-1,3-propanediones vol.33, pp.4, 2012, https://doi.org/10.5012/bkcs.2012.33.4.1379
- -(Alkynon-1-yl)phenols vol.39, pp.9, 2018, https://doi.org/10.1002/bkcs.11557
- An Efficient One-Pot Synthesis and Anticancer Activity of 4'-Substituted Flavonoids vol.88, pp.5, 2018, https://doi.org/10.1134/S1070363218050328
- Fine tuning of a reported synthetic route for biologically active flavonoid, baicalein vol.30, pp.1, 2007, https://doi.org/10.1007/BF02977773
- A New Route for the Synthesis of Flavanones from 2-Methoxybenzoic Acids vol.26, pp.12, 2005, https://doi.org/10.5012/bkcs.2005.26.12.2044
- A Novel Synthesis of Flavones from 2-Methoxybenzoic Acids. vol.37, pp.7, 2006, https://doi.org/10.1002/chin.200607144
- Mechanically Activated Solid-State Synthesis of Flavones by High-Speed Ball Milling vol.39, pp.23, 2005, https://doi.org/10.1080/00397910902898551
- 2'-하이드록시아세토페논으로부터 고리-A 하이드록시플라본의 효과적 합성 vol.53, pp.3, 2005, https://doi.org/10.5012/jkcs.2009.53.3.382
- Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives vol.8, pp.None, 2005, https://doi.org/10.3762/bjoc.8.244
- Part II: nitroalkenes in the synthesis of heterocyclic compounds vol.4, pp.93, 2005, https://doi.org/10.1039/c4ra08830a
- Peptoid Helix Displaying Flavone and Porphyrin: Synthesis and Intramolecular Energy Transfer vol.85, pp.3, 2020, https://doi.org/10.1021/acs.joc.9b02358
- Halogenated Flavones and Isoflavones: A State-of-Art on their Synthesis vol.17, pp.6, 2005, https://doi.org/10.2174/1570179417666200530213737