PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Czasopismo
2010 | 8 | 1 | 174-181
Tytuł artykułu

Synthesis and characterization of some chalcones and their cyclohexenone derivatives

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A series of chalcones and their derivatives have been synthesized. Chalcones, 1-(1,3-benzodioxol-5-yl)-3-(aryl)-prop-2-en-1-ones were prepared by the aldol condensation of 1-(1,3-benzodioxol-5-yl)ethanones and aryl aldehydes. Based-catalyzed condensation of 1-(1,3-benzodioxol-5-yl)-3-(aryl)prop-2-en-1-ones with ethyl acetoacetate yields corresponding ethyl 4-(1,3-benzodioxol-5-yl)-6-(aryl)-2-oxocyclohex-3-ene-1-carboxylates. Some of the synthesized chalcones were reported in the literature; the newly synthesized compounds were characterized by single crystal X-ray studies, IR, 1H-NMR and LCMS mass spectral analysis. [...]
Wydawca

Czasopismo
Rocznik
Tom
8
Numer
1
Strony
174-181
Opis fizyczny
Daty
wydano
2010-02-01
online
2010-02-16
Twórcy
  • Department of Post-Graduate Studies and Research in Chemistry, Mangalore University, Mangalagangotri, 574 199, India
  • Department of Post-Graduate Studies and Research in Chemistry, Mangalore University, Mangalagangotri, 574 199, India, nbadiadka@yahoo.co.uk
  • Department of Studies in Chemistry, University of Mysore, Mysore, 570 006, India
Bibliografia
  • [1] D.N. Dhar, The Chemistry and Related Compounds (John Wiley, New York, 1981)
  • [2] Z. Nowakowska, Eur. J. Med. Chem. 42, 125 (2007) http://dx.doi.org/10.1016/j.ejmech.2006.09.019[Crossref]
  • [3] S. Lopez et al., Bioorg. Med. Chem. 9, 1999 (2001) http://dx.doi.org/10.1016/S0968-0896(01)00116-X[Crossref]
  • [4] P. Boeck et al., Arch Pharmacy 338, 87 (2005) http://dx.doi.org/10.1002/ardp.200400929[Crossref]
  • [5] H.N. Elsohly, A.S. Joshi, A.C. Nimrod, L.A. Walker, A.M. Clark, Planta Medica 67, 87 (2001) http://dx.doi.org/10.1055/s-2001-10621[Crossref]
  • [6] N. Yayli et al., J. Photochem.Photobiol. A 169, 229 (2005) http://dx.doi.org/10.1016/j.jphotochem.2004.06.015[Crossref]
  • [7] M.V.B. Reddy et al., Bioorg. Med. Chem. 16, 7358 (2008) http://dx.doi.org/10.1016/j.bmc.2008.06.018[Crossref]
  • [8] G. Saydam et al., Lukemia Research 27, 57 (2003) http://dx.doi.org/10.1016/S0145-2126(02)00058-9[Crossref]
  • [9] M. Cabrera et al., Bioorg. Med. Chem. 15, 356(2007) http://dx.doi.org/10.1016/j.bmc.2007.03.031[Crossref]
  • [10] C. Nakamura et al., Bioorg. Med. Chem. 10, 699 (2002) http://dx.doi.org/10.1016/S0968-0896(01)00319-4[Crossref]
  • [11] A. Modzelewska, C. Pettit, G. Achanta, N.E. Davidson, P. Huang, S.R. Khan, Bioorg. Med. Chem. 14, 3491 (2006) http://dx.doi.org/10.1016/j.bmc.2006.01.003[Crossref]
  • [12] D.J. Kerr, E. Hamel, M.K. Jung, B.L. Flynn, Bioorg. Med. Chem. 15, 3290 (2007) http://dx.doi.org/10.1016/j.bmc.2007.02.006[Crossref]
  • [13] D.Y. Kim et al., J.Med. Chem. 49, 5664 (2006) http://dx.doi.org/10.1021/jm050761i[Crossref]
  • [14] N.J. Lawrence, R.P. Patterson, L.-L. Ooi, D. Cook, S. Ducki, Bioorg. Med. Chem. Lett. 16, 5844 (2006) http://dx.doi.org/10.1016/j.bmcl.2006.08.065[Crossref]
  • [15] J.A. Hadfield, S. Ducki, N. Hirst, A.T. McGown, Progress in Cell Cycle Research 5, 309 (2003)
  • [16] M.L. Edwards, S.P. Sunkara, D.M. Stemerick, US Patent No. 4863968, 1989.09.05.
  • [17] M.D. Aggarwal, W.S. Wang, K. Bhat, B.G. Penn, D.O. Frazeir, In: H.S. Nalwa (Ed.), Handbook of Advanced Electronic and Photonic Materials and Devices (Academic Press, USA, 2001) Vol. 9, 193 http://dx.doi.org/10.1016/B978-012513745-4/50075-5
  • [18] M. Samoc, A. Samoc, B. Luther-Davies, J. Opt. Soc. Am. B 15, 817 (1998) http://dx.doi.org/10.1364/JOSAB.15.000817[Crossref]
  • [19] J. Indira, P.P. Karat, B.K. Sarojini, J. Cryst. Growth 242, 209 (2002) http://dx.doi.org/10.1016/S0022-0248(02)01306-4[Crossref]
  • [20] L. Troeberg et al., Mol. Med. 6, 660 (2000)
  • [21] V.J. Ram, A.X. Saxena, S. Srivastava, S. Chandra, Bioorg. Med. Chem. Lett. 10, 2159 (2000) http://dx.doi.org/10.1016/S0960-894X(00)00409-1[Crossref]
  • [22] M. Chen, T.G. Theander, S.B. Christensen, L. Hviid, L. Zhai, A. Kharazmi, Antimicrobial Agents and Chemotherapy 38, 1470 (1994) [Crossref]
  • [23] A. Kharazmi, M. Chen, T. Theander, S.B. Christensen, Annals Trop. Med. Parasite. 91, S91 (1997) http://dx.doi.org/10.1080/00034989761364[Crossref]
  • [24] Z. Zhang, Y.W. Dong, G.W. Wang, Chem. Lett. 33, 168 (2004) http://dx.doi.org/10.1246/cl.2004.168[Crossref]
  • [25] J-C. Jung et al., J. Med. Chem. 51, 4054 (2008) http://dx.doi.org/10.1021/jm800221g[Crossref]
  • [26] M.K. Ruby, R. Venkataramanan, Chem. Heterocycl. Comp. 40, 631(2004) http://dx.doi.org/10.1023/B:COHC.0000037319.75957.fb[Crossref]
  • [27] B. Insuasty, F. Orozco, J. Quiroga, R. Abonia, M. Nogueras, J. Cobo, Eur. J. Med. Chem. 43, 1955 (2008) http://dx.doi.org/10.1016/j.ejmech.2007.12.005[Crossref]
  • [28] B. Lygo, S.D. Gardiner, M.C. McLeod, D.C.M. To, Org. Biomol. Chem. 5, 2283 (2007) http://dx.doi.org/10.1039/b706546a[Crossref]
  • [29] J.P. Jasinski, R.J. Butcher, T.V. Sreevidya, H.S. Yathirajan, B. Narayana, Analytical Sciences, 24, x245 (2008)
  • [30] H. Li, T.V. Sreevidya, B. Narayana, B.K. Sarojini, H.S. Yathirajan, Acta Crystallographica, E64, o2387 (2008)
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_s11532-009-0124-x
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.