[1]. Anastas P.T., Kirchhoff M.M. Acc. Cheme. Res., 2002, 35:686
[2]. Menger F.M., Chem. Soc. Rev., 1972, 1:229
[3]. Starks C.M. J. Am. Chem. Soc., 1971, 93:195
[4]. Izatt R.M., Pawlak K., Bradshaw J.S., Bruening R.L. Chem. Rev.,1991, 91:1721
[5]. Jayachandran J.P., Wang M.L. Appl. Catal. A: Gen., 2000, 198:67
[6]. Fiamegos Y.C., Stalikas C.D. Anal. Chin. Acta., 2005, 550:1
[7]. Makossa M. ACS Symp. Ser., 1996, 41:626
[8]. Harmer M.A., Sun Q. Appl. Catal. A: Gen., 2001, 221:45
[9]. Yadav G.D., Lande S.V. Appl. Catal. A: Gen., 2005, 287:267
[10]. Huang C.C., Yang H.M. Appl. Catal. A: Gen., 2005, 290:65
[11]. Baj S., Siewniak A., Socha B. Appl. Catal. A: Gen., 2006, 309:85
[12]. Balakrishnan T., Murugan E., Siva A. Appl. Catal. A: Gen., 2004, 273:89
[13]. Taha N., Sasson Y., Chidambaram M. Appl. Catal. A: Gen., 2008, 350:217
[14]. Albanes D. Catal. Rev., 2003, 45:369
[15]. Jwo J.J. Catal. Rev., 2003, 45:397
[16]. Yang H.M., Wu H.S. Catal. Rev., 2003, 45:463
[17]. Albanese D., Landini D., Maia A., Penso M. J. Mol. Catal. A: Chem., 1999, 150:113
[18]. Naik S.D., Doraiswamy L.K. AIChE Journal., 1998, 44:612
[19]. Balakrishnan T., Jayachandran J.P. ACS. Symp. Ser., 1997, 659:277
[20]. Yadav G.D., Lande S.V. Adv. Synth. Catal., 2005, 347:1235
[21]. Makosza M. Pure Appl. Chem., 2000, 72:1399
[22]. Idoux J.P., Wysocki R., Young S., Turcot J., Ohlman C., LeonardR. Synth. Commun., 1983, 13:139
[23]. Wang M.L., Lee Z.F. Ind. Eng. Chem. Res., 2006, 45:4918
[24]. Bender J., Jepkens D., Husken H. Org. Proc. Res & Dev., 2010, 14:716
[25]. Yadav G.D., Desai N.M. J. Mol. Catal. A: Chem., 2006, 243:278
[26]. Benaglia M., Cinquini M., Cozzi F., Tocco G. Tetrahedron Lett., 2002, 43:3391
[27]. Jew S., Jeong B., Yoo M., Huh H., Park H. Chem. Commun., 2001, 14:1244
[28]. Chinchilla R., Mazon P., Najera C. Tetrahedron Asymmetry., 2002, 13:927
[29]. Park H., Jeong B.S., Yoo M.S., Lee J.H., Park B.S., Kim M.G., Jew S.S. Tetrahedron. Lett., 2003, 44:497
[30]. Jayachandran J.P., Wheelet C., Eason B.C., Liotta C.L., Eckert C.A., Supercrit. J. Fluid., 2003, 27:179
[31]. Teoh S.G., Ang S.H., Fun H.K., Ong C.W. Organomet. Chem., 1999, 580:17
[32]. Basu Baul T.S., Mizar A., Lycka A., Rivarola E., Jirasko R., Holcapek M., Vos D.D., Englert U. J. Organomet. Chem., 2006, 691:3416
[33]. Muller T.E., Beller M. Chem. Rev., 1998, 98:675
[34]. Rabonivite M., Sasson Y., Halpern M. J. Org. Chem., 1983, 48:1022
[35]. Ali H.E.S. Catalysis Commun., 2007, 8:855
[36]. Solaro R., Antone S.D., Chiellini E.G. J. Org. Chem., 1980, 45:4179
[37]. Jayachandran J.P., Wang M.L. Appl. Catal. A: Gen., 2001, 319:11
[38]. Murugan E., Gopinath P. Appl. Catal. A: Gen., 2007, 319:72
[39]. Wang M.L., Chen C.J. Org. Proc. Res & Dev., 2010, 14:737
[40]. Wang M.L., Rajndran V. UltraSon. Sonochem., 2007, 14:368
[41]. Wang M.L. Tseng Y.H. J. Mol. Catal. A: Chem., 2002, 188:51
[42]. Wu H.S., Lai J.J. Ind. Eng. Chem & Res., 1995, 34:1536
[43]. Rabinoviz M., Cohen Y., Halpern M. Angew. Chem. Int. Ed. Engl.,1986, 25:960
[44]. Acker R.D. Tetrahedron Lett., 1978, 19:2399
[45]. Tomoi M., Ford W.T. J. Am. Chem. Soc., 1981, 103:3821
[46]. Sasson Y., Bilman N. J. Chem. Soc. Perkin Trans., 1989, 2:2029
[47]. Yadav G.D., Bisht P.M. J. Mol. Catal. A: Chem., 2004, 223:93