References
- Ellis, G. P. Chromenes, Chromanones, and Chromones in The Chemistry of Heterocyclic Compounds; Wiley: New York, 1977; Vol. 31, p 11
- Hepworth, J. Comprehensive Heterocyclic Chemistry; Katrizky, A. R., Rees, C. W., Eds.; Pergamon: Oxford, UK, 1984; Vol. 3, p 737
- Davis, M.; Pettett, M. Aust. J. Chem. 1979, 32, 369 https://doi.org/10.1071/CH9790369
- Rustaiyan, A.; Nazarians, L.; Bohlmann, F. Phytochemistry 1980, 19, 1254 https://doi.org/10.1016/0031-9422(80)83104-9
- Kamperdick, C.; Van, N. H.; Sung, T. V.; Adam, G. Phytochemistry 1997, 45, 1049 https://doi.org/10.1016/S0031-9422(97)00059-9
- Cambie, R. C.; Pan, Y. J.; Bowden, B. F. Biochem. System. Ecol. 1996, 24, 461 https://doi.org/10.1016/0305-1978(96)88874-0
- Muyard, F.; Bissoue, A. N.; Bevalot, F.; Tillequin, F.; Cabalion, P.; Vaquette, J. Phytochemistry 1996, 42, 1175 https://doi.org/10.1016/0031-9422(96)00077-5
- McKee, T.; Fuller, R. W.; Covington, C. D.; Cardellina II, J. H.; Gulakowski, R. J.; Krepps, B. L.; McMahon, J. B.; Boyd, M. R. J. Nat. Prod. 1996, 59, 754 https://doi.org/10.1021/np9603784
- Galinis, D. L.; Fuller, R. W.; McKee, T. C.; Cardellina II, J. H.; Gulakowski, R. J.; McMahon, J. B.; Boyd, M. R. J. Med. Chem. 1996, 39, 4507 https://doi.org/10.1021/jm9602827
- Cardellina, J. H.; Bokesch, H. R.; McKee, T. C.; Boyd, M. R. Bioorg. Med. Chem. Lett. 1995, 5, 1011 https://doi.org/10.1016/0960-894X(95)00158-P
- Lee, Y. R.; Choi, J. H.; Yoon, S. H. Tetrahedron Lett. 2005, 46, 7539 https://doi.org/10.1016/j.tetlet.2005.08.159
- Lee, Y. R.; Kim, D. H. Synthesis 2006, 603
- Lee, Y. R.; Lee, W. K.; Noh, S. K.; Lyoo, W. S. Synthesis 2006, 853
- Lee, Y. R.; Wang, X. Bull. Korean Chem. Soc. 2005, 26, 1933 https://doi.org/10.5012/bkcs.2005.26.12.1933
- Wang, X.; Lee, Y. R. Synthesis 2007, 3044
- Lee, Y. R.; Xia, L. Synthesis 2007, 3244
- Wang, X.; Lee, Y. R. Tetrahedron Lett. 2007, 48, 6275 https://doi.org/10.1016/j.tetlet.2007.07.022
- Lee, Y. R.; Kim, J. H. Synlett 2007, 2232
- Saimoto, H.; Yoshida, K.; Murakami, T.; Morimoto, M.; Sashiwa, H.; Shigemasa, Y. J. Org. Chem. 1996, 61, 6768 https://doi.org/10.1021/jo961352k
- Crombie, L.; Redshaw, S. D.; Whiting, D. A. J. Chem. Soc. Chem. Commun. 1979, 630
- Olivares, E, M.; Gonzalez, J. G.; Monache, F. D. Phytochemistry 1994, 36, 473 https://doi.org/10.1016/S0031-9422(00)97098-5
- Khattri, P. S.; Sahai, M.; Dasgupta, B.; Ray, A. B. Heterocycles 1984, 22, 249 https://doi.org/10.3987/R-1984-02-0249
- Lin, Y. L.; Chen, Y. L.; Kuo, Y. H. Chem. Pharm. Bull. 1992, 40, 2295 https://doi.org/10.1248/cpb.40.2295
- Cao, S.; Schilling, J. K.; Miller, J. S.; Andriantsiferana, R.; Rasamison, V. E.; Kingston, D. G. I. J. Nat. Prod. 2004, 67, 454 https://doi.org/10.1021/np0303815
- Donnelly, W. J. G.; Shannon, P. V. R. J. Chem. Soc. Perkin Trans. 1 1972, 25 https://doi.org/10.1039/p19720000025
- Pernin, R.; Muyard, F.; Bevalot, F.; Tillequin, F.; Vaquette, J. J. Nat. Prod. 2000, 63, 245 https://doi.org/10.1021/np9902845
- Basaif, S. A.; Sobahi, T. R.; Khalil, A. K.; Hassan, M. A. Bull. Korean Chem. Soc. 2005, 26, 1677 https://doi.org/10.5012/bkcs.2005.26.11.1677
- Deodhar, M.; Black, D. S.; Kumar, N. Org. Prep. Proc. Int. 2006, 38, 94
Cited by
- ]chromen-6-yl)ethanone vol.68, pp.10, 2012, https://doi.org/10.1107/S160053681204055X
- ]chromen-6-yl)-3-(4-methoxyphenyl)prop-2-en-1-one vol.69, pp.4, 2013, https://doi.org/10.1107/S1600536813005734
- ]chromene Derivatives vol.52, pp.1, 2014, https://doi.org/10.1002/jhet.1991
- Visible light promoted synthesis of dihydropyrano[2,3-c]chromenes via a multicomponent-tandem strategy under solvent and catalyst free conditions vol.18, pp.11, 2016, https://doi.org/10.1039/C5GC02855H
- ChemInform Abstract: An Efficient and Concise Synthesis of Biologically Interesting Pyranochromenes by Ethylenediamine Diacetate-Catalyzed Double Condensation of Substituted Trihydroxybenzenes to α,β-Unsaturated Aldehydes and Application to Natural Product Analogues. vol.39, pp.10, 2008, https://doi.org/10.1002/chin.200810134
- A New Synthetic Route for Natural Products with the Pyranobenzophenone Moiety: Clusiacitran A, Vismiaphenone B, Isovismiaphenone B, and Myrtiaphenone B vol.29, pp.2, 2007, https://doi.org/10.5012/bkcs.2008.29.2.515
- First Concise Total Syntheses of Biologically Interesting Nicolaioidesin C, Crinatusin C1, and Crinatusin C2 vol.29, pp.6, 2007, https://doi.org/10.5012/bkcs.2008.29.6.1199
- Concise Total Synthesis of Biologically Interesting Prenylated Chalcone Natural Products: 4'-O-Methylxanthohumol, Xanthohumol E, and Sericone vol.29, pp.6, 2007, https://doi.org/10.5012/bkcs.2008.29.6.1205
- New and General Methods for the Synthesis of Arylmethylene Bis(3-Hydroxy-2-Cyclohexene-1-Ones) and Xanthenediones by EDDA and In(OTf)3-Catalyzed One-Pot Domino Knoevenagel/Michael or Koeven vol.30, pp.9, 2007, https://doi.org/10.5012/bkcs.2009.30.9.1989
- Synthesis and structure elucidation of a series of pyranochromene chalcones and flavanones using 1D and 2D NMR spectroscopy and X‐ray crystallography vol.52, pp.6, 2007, https://doi.org/10.1002/mrc.4062
- Synthesis of Chromenes by Cyclizative Condensation of Phenols with α,β-Unsaturated Carbonyl Compounds over Halide Cluster Catalysts vol.45, pp.11, 2007, https://doi.org/10.1246/cl.160681