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Synthesis and NMR of 4-Aryl-3,4-dihydrocoumarins and 4-Arylcoumarins
Corresponding Author(s) : Jie Sun
Asian Journal of Chemistry,
Vol. 26 No. 22 (2014): Vol 26 Issue 22
Abstract
This paper described the synthesis and 1H and 13C NMR chemical shifts of a series of 4-aryl-3,4-dihydrocoumarin and 4-arylcoumarin derivatives based on a combination of 1H and 13C NMR, HSQC and HMBC experiments.
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- J. Guerrero-Analco, O. Medina-Campos, F. Brindis, R. Bye, J. Pedraza-Chaverri, A. Navarrete and R. Mata, Phytochemistry, 68, 2087 (2007); doi:10.1016/j.phytochem.2007.05.006.
- T.C. Taechowisan, P. Tuntiwachwuttikul, C.H. Lu, Y.M. Shen, S. Lumyong and W.C. Taylor, Immun. Inv., 36, 203 (2007); doi:10.1080/08820130600992115.
- T.C. Taechowisan, C.H. Lu, Y.M. Shen and S. Lumyong, Nat. Prod. Res., 21, 1104 (2007); doi:10.1080/14786410601129671.
- C. Bailly, C. Bal, P. Barbier, S. Combes, J.P. Finet, M.P. Hildebrand, V. Peyrot and N. Wattez, J. Med. Chem., 46, 5437 (2003); doi:10.1021/jm030903d.
- E. Rizzi, S. Dallavalle, L. Merlini, G. Pratesi and F. Zunino, Synth. Commun., 36, 1117 (2006); doi:10.1080/00397910500501235.
- O.G. Ganina, E. Daras, V. Bourgarel-Rey, V. Peyrot, A.N. Andresyuk, J.-P. Finet, A.Y. Fedorov, I.P. Beletskaya and S. Combes, Bioorg. Med. Chem., 16, 8806 (2008); doi:10.1016/j.bmc.2008.09.003.
- T.C. Taechowisan, C.H. Lu, Y.M. Shen and S. Lumyong, Microbiology, 151, 1691 (2005); doi:10.1099/mic.0.27758-0.
- J. Sun, W.X. Ding, K.Y. Zhang and Y. Zou, Chin. Chem. Lett., 22, 667 (2011); doi:10.1016/j.cclet.2010.12.017.
References
J. Guerrero-Analco, O. Medina-Campos, F. Brindis, R. Bye, J. Pedraza-Chaverri, A. Navarrete and R. Mata, Phytochemistry, 68, 2087 (2007); doi:10.1016/j.phytochem.2007.05.006.
T.C. Taechowisan, P. Tuntiwachwuttikul, C.H. Lu, Y.M. Shen, S. Lumyong and W.C. Taylor, Immun. Inv., 36, 203 (2007); doi:10.1080/08820130600992115.
T.C. Taechowisan, C.H. Lu, Y.M. Shen and S. Lumyong, Nat. Prod. Res., 21, 1104 (2007); doi:10.1080/14786410601129671.
C. Bailly, C. Bal, P. Barbier, S. Combes, J.P. Finet, M.P. Hildebrand, V. Peyrot and N. Wattez, J. Med. Chem., 46, 5437 (2003); doi:10.1021/jm030903d.
E. Rizzi, S. Dallavalle, L. Merlini, G. Pratesi and F. Zunino, Synth. Commun., 36, 1117 (2006); doi:10.1080/00397910500501235.
O.G. Ganina, E. Daras, V. Bourgarel-Rey, V. Peyrot, A.N. Andresyuk, J.-P. Finet, A.Y. Fedorov, I.P. Beletskaya and S. Combes, Bioorg. Med. Chem., 16, 8806 (2008); doi:10.1016/j.bmc.2008.09.003.
T.C. Taechowisan, C.H. Lu, Y.M. Shen and S. Lumyong, Microbiology, 151, 1691 (2005); doi:10.1099/mic.0.27758-0.
J. Sun, W.X. Ding, K.Y. Zhang and Y. Zou, Chin. Chem. Lett., 22, 667 (2011); doi:10.1016/j.cclet.2010.12.017.