References
- Desideri, N.; Conti, C.; Mastropaolo, F. Antiviral Chem. Chemother. 2000, 11, 373
- Peixoto, F.; A. Barros, I. R. N. A.; Silva, A. M. S. J. Biochem. Mol. Toxicol. 2002, 16, 220 https://doi.org/10.1002/jbt.10042
- Fernandes, E.; Carvalho, M.; Carvalho, F.; Silva, A. M. S.; Santos, C. M. M.; Pinto, D. C. G. A.; Cavaleiro, J. A. S.; Bastos, M. L. Arch. Toxicol. 2003, 77, 500 https://doi.org/10.1007/s00204-003-0480-9
- Filipe, P.; Silva, A. M. S.; Morlière, P.; Brito, C. M.; Patterson, L. K.; Hug, G. L.; Silva, J. N.; Cavaleiro, J. A. S.; Mazière, J.-C.; Freitas, J. P.; Santus, R. Biochem. Pharmacol. 2004, 67, 2207 https://doi.org/10.1016/j.bcp.2004.02.030
- (a) Doria, G.; Romero, C.; Forgione, A.; Sberze, P.; Tibolla, N.; Corno, M. L.; Cruzzola, G.; Cadelli, G. Eur. J. Med. Chem. 1979, 14, 347.(Please refer to the other references for details:no.24)
- (a) Gerwick, W. H.; Lopez, A.; Van Duyne, G. D.; Clardy, J.; Ortiz, W.; Baez, A. Tetrahedron Lett. 1986, 27, 1979. (Please refer to the other references for details:no.25) https://doi.org/10.1016/S0040-4039(00)84426-3
- Sonawane, S. A.; Chavan, V. P.; Karale, B. K.; Shingare, M. S. Ind. J. Heterocyclic Chem. 2002, 12, 65
- (a) Karale, B. K.; Gill, C. H.; Shingare, M. S. Ind. J. Heterocycl. Chem. 2003, 12, 267. (Please refer to the other references for details:no.26) https://doi.org/10.1002/jhet.5570120211
- Sandulache, A.; Silva, A. M. S.; Pinto, D. C. G. A.; Almeida, L. M. P. M.; Cavaleiro, J. A. S. New J. Chem. 2003, 27, 1592 https://doi.org/10.1039/b303554a
- Lokshin, V.; Heynderickx, A.; Samat, A.; Pèpe, G.; Guglielmetti, R. Tetrahedron Lett. 1999, 40, 6761 https://doi.org/10.1016/S0040-4039(99)01301-5
- Atassi, G.; Briet, P.; Berthelon, J. P.; Collonges, F. J. Med. Chem. Chim. Ther. 1985, 20, 393
- Middleton, Jr., E.; Kandaswami, C. The Flavonoids Advances in Research Since 1986; Harborne, J. B., Ed.; Chapman: Hall, London, 1994; p 619
- Harborne, J. B.; Williams, C. A. Phytochemistry 2000, 55, 481 https://doi.org/10.1016/S0031-9422(00)00235-1
- Thomas, W. Chem. Rev. 1999, 99, 2071 https://doi.org/10.1021/cr980032t
- Sheldon, R. Chem. Commun. 2001, 2399 https://doi.org/10.1039/b107270f
- Zhao, D.; Wu, M.; Kou, Y.; Min, K. Catal. Today 2002, 2654, 1
- Peng, J.; Deng, Y. Tetrahedron Lett. 2001, 42, 403 https://doi.org/10.1016/S0040-4039(00)01974-2
- Shen, Z. L.; Zhou, W. J.; Liu, Y. T.; Ji, S. J.; Loh, T. P. Green Chem. 2008, 10, 283 https://doi.org/10.1039/b717235d
- Gong, K.; He, Z.-W.; Xu, Y.; Fang, D.; Liu, Z.-L. Monatsh. Chem. 2008, 139, 913 https://doi.org/10.1007/s00706-008-0871-y
- (a) Fischer, T.; Sethi, A.; Welton, T.; Woolf, J. Tetrahedron Lett. 1999, 40, 793.(Please refer to the other references for details:no.27-no.28) https://doi.org/10.1016/S0040-4039(98)02415-0
- Kahveci, B.; Ozil, M.; Serdar, M. Heteroatom Chem. 2008, 19, 38 https://doi.org/10.1002/hc.20381
- (a) Karale, B. K.; Chavan, V. P.; Mane, A. S.; Hangarge, R. V.; Gill, C. H.; Shingare, M. S. Synth. Comm. 2002, 32, 497.(Please refer to the other references for details:no.29-no.30) https://doi.org/10.1081/SCC-120002395
- (a) Pawar, S. S.; Dekhane, D. V.; Shingare, M. S.; Thore, S. N. Tetrahedron Lett. 2008, 49, 4252.(Please refer to the other references for details:no.31-no.36) https://doi.org/10.1016/j.tetlet.2008.04.148
- (b) Brion, J. D.; Le Baut, G.; Zammattio, F.; Pierre, A.; Atassi, G.; Belachmi, L. Eur. Pat. Appl. 1991, EP 454, 587; Chem. Abstr. 1992, 116, 106092K
- (b) Gerwick, W. H. J. Nat. Prod. 1989, 52, 252 https://doi.org/10.1021/np50062a005
- (b) Silva, V. L. M.; Silva, A. M. S.; Pinto, D. C. G. A.; Cavaleiro, J. A. S. Aveiro. 2003, PO102, 148
- (b) Le Boulaire, V. R. Chem. Commun. 2000, 2195. https://doi.org/10.1039/b006666o
- (c) Ji, S. J.; Jiang, Z. Q.; Lu, J.; Loh, T. P Synlett 2004, 5, 831. https://doi.org/10.1055/s-2004-820035
- (b) Shindalkar, S. S.; Madje, B. R.; Shingare, M. S. Mendeleev Commun. 2007, 17, 43. https://doi.org/10.1016/j.mencom.2007.01.017
- (c) Sapkal, S. B.; Shelke, K. F.; Shingate, B. B.; Shingare, M. S. Tetrahedron Lett. 2009, 50, 1754. https://doi.org/10.1016/j.tetlet.2009.01.140
- (b) Sadaphal, S. A.; Shelke, K. F.; Sonar, S. S.; Shingare, M. S. Central Euro. J. Chem. 2008, 6, 622. https://doi.org/10.2478/s11532-008-0069-5
- (c) Diwakar, S. D.; Bhagwat, S. S.; Shingare, M. S.; Gill, C. H. Bioorg. Med. Chem. Lett. 2008, 18, 4678. https://doi.org/10.1016/j.bmcl.2008.07.007
- (d) Shelke, K. F.; Sapkal, S. B.; Shingare, M. S. Chie. Chem. Lett. 2009, 20, 283. https://doi.org/10.1016/j.cclet.2008.11.033
- (e) Shelke, K. F.; Sapkal, S. B.; Sonar, S. S.; Madje, B. R.; Shingate, B. B.; Shingare, M. S Bull. Korean Chem. Soc. 2009, 30, 1057. https://doi.org/10.5012/bkcs.2009.30.5.1057
- (f) Shelke, K. F.; Madje, B. R.; Sapkal, S. B.; Shingate, B. B.; Shingare, M. S. Green Chem. Lett. Rev. 2009, 2, 3. https://doi.org/10.1080/17518250902763101
- (e) Shelke, K. F.; Sapkal, S. B.; Kategaonkar, A. H.; Shingate, B. B.; Shingare, M. S. S. Afr. J. Chem. 2009, 62, 109.
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