[1] (a) T. Ratan Bal, B. Anand, P. Yogeeswari, D.H. Sriram, Bioorg. Med. Chem. Lett. 15 (2005) 4451–4455. (b) T. Jiang, K.L. Kuhen, K. Wolff, H. Yin, K. Ieza, J. Caldwell, B. Bursulaya, T.Tuntland, K. Zhang, D. Karanewsky, Y. He, Bioorg. Med. Chem. Lett. 16 (2006) 2109–2112.
[2] R. Tripathy, A. Reiboldt, P.A. Messina, M. Iqbal, J. Singh, E.R. Bacon, S. Angeles, Sh.X. Yang, M.S. Albom, C. Robinson, H. Chang, B.A. Ruggeri, J.P. Mallamo, Bioorg. Med. Chem. Lett. 16 (2006) 2158–2162.
[3] (a) A. Cane, M.C. Tournaire, D. Barritault, M. Crumeyrolle-Arias, Biochem. Biophys. Res. Commun. 276 (2000) 379–384. (b) V.C. Silveira, J.S. Luz, C.C. Oliveira, I. Graziani, M.R. Ciriolo, A.M. C. Ferreira, J. Inorg. Biochem. 102 (2008) 1090–1103.
[4] (a) A. Amal Raj, R. Raghunathan, M.R. Sridevikumaria, N. Raman, Bioorg. Med. Chem. 11 (2003) 407–419. (b) M.C. Rodriguez-Arguelles, S. Mosquera-Vazaquez, P. Touron-Touceda, J. Sanmartin-Matalobos, A.M. Garcia-Deibe, M. Belicchi-Ferraris, G. Pelosi, C. Pelizzi, F.J. Zani, J. Inorg. Biochem. 101 (2007) 138–147.
[5] L. Maskell, E.A. Blanche, M.A. Colucci, J.L. Whatmore, Ch. Moody J. Bioorg. Med. Chem. Lett. 17 (2007) 1575–1578.
[6] (a) R. Shimazawa, M. Kuriyama, R. Shirai, R. Bioorg. Med. Chem. Lett. 18 (2008) 3350–3353.
(b) A.H. Abadi, S.M. Abou-Seri, D.E. Abdel-Rahman, Ch. Klein, O. Lozach, L. Meijer, Eur. J. Med. Chem. 41(2006) 296–305.
[7] (a) Y. Yamada, M. Kitajima, N. Kogure, H. Takayama, Tetrahedron 64 (2008) 7690–7694.
(b) N. Kogure, H. Kobayashi, N. Ishii, M. Kitajima, S. Wongseripipatana, H. Takayama, Tetrahedron Lett. 49 (2008) 3638–3642. (c) Z. Zhang, Y. T. Di, Y. T. Wang, S. Z. Mu, X. Fang, Y. Zhang, C. J. Tan, Q. Zhang, X. H.Yan, J. Guo, Tetrahedron 65 (2009) 4551–4556. (d) T.S. Kam, Y.M. Choo, Tetrahedron 56 (2000) 6143–6150. (e) Y. Wu, M. Kitajima, N. Kogure, R. Zhang, H. Takayama, Tetrahedron Lett. 49 (2008) 5935–5938.
[8] W.J. Skiles, D. McNeil, R.B. Labroo, E.A. Cohen, J. Org. Chem. 64 (1999) 1369-1371.
[9] (a) J.I. Jimenez, U. Huber, R.E. Moore, G.M.L. Patterson, J. Nat. Prod. 62 (1999) 569-572. (b) H.B. Rasmussen, J.K. MacLeod, J. Nat. Prod. 60 (1997) 1152-1154. (c) T. Tokunaga, W.E. Hume, T. Umezome, K. Okazaki, Y. Ueki, K. Kumagai, S. Hourai, J. Nagamine, H. Seki, M. Taiji, H. Noguchi, R. Nagata, J. Med. Chem. 44 (2001) 4641-4649. (d) J. Nagamine, R. Nagata, H. Seki, N. Nomura-Akimaru, Y. Ueki, K. Kumagai, M. Taiji, H. Noguchi, J. Endocrinol. 171 (2001) 481-489.
[10] (a) F. Imre, N. Miklo's, S. Aron, B. Ga'bor, T. La'szlo', Tetrahedron 57 (2001) 1129-1137. (b) D.R. Long, C.G. Richards, M.S.F. Ross, J. Hetrocycl. Chem. 15 (1978) 633-677. (c) F.A. Luzziao, Tetrahedron 57 (2001) 915-1138.
[11] L. Liu, S. Zhang, F. Xue, G. Lou, H. Zhang, S. Ma, W. Duan, Chem. Eur. J. 17 (2011) 1791-1795.
[12] G. Chen, Y. Wang, H. He, S. Gao, X. Yang, X. Hao, Heterocycles 68 (2006).2327–2333.
[13] W.R. Conn, H.G. Lindwall, J. Am. Chem. Soc. 58 (1936) 1236–1239.
[14] G. Chen, X-J. Hao, Q-Y. Sun, J. Ding, Chemical Papers 64 (2010) 673-677.
[15] H.M. Meshram, Palakuri Ramesh, A. Sanjeeva Kumar, A. Swetha, Tetrahedron Lett. 52 (2011) 5862–5864.
[16] H.M. Meshram, B.P. Thakur, M.B. Bejjam, V.M. Bangade, Green Chem. Lett. & Rev. 6 (2013) 19-43.
[17] M.N. Elinson, A.I. Ilovaisky, V.M. Merkulova, F. Barba, B. Batanero, B. Tetrahedron 64 (2008) 5915–5919.
[18] (a) P. Wasserscheid, T. Welton, Ionic Liquids in Synthesis; Wiley-VCH Verlag: Stuttgart, Germany, 2002. (b) M. Fremantle, Chem. Eng. News 76 (1998) 32-37.
[19] N.M.M. Mateus, L.C. Branco, N.M.T. Lourenco, C.A.M. Afonso, Green Chem. 5 (2003) 347–352.
[20] (a) K. Rad-Moghadam, L. Youseftabar-Miri, J. Florin. Chem. 135 (2012) 213-219. (b) H. Hosseinjani-Pirdehi, K. Rad-Moghadam, L. Youseftabar-Miri, Tetrahedron 70 (2014) 1780-1785. (c) K. Rad-Moghadam, L. Youseftabar-Miri, Arkivoc XI (2011) 43-50. (d) K. Rad-Moghadam, L. Youseftabar-Miri, Tetrahedron 67 (2011) 5693-5699
[21] E. Hosseini, K. Karimzadeh, M. Vessal, M. Rafieirad, HealthMED. J. 612 (2012) 4253-4257.
[22] S. Lenzen, Diabetologia 51 (2008) 216-226.
)