[1] Fringuelli F., Taticchi A. The Diels-Alder Reaction. Selected Practical Methods; John Wiley & Sons: New York, 2002
[2] Fleming I. Pericyclic Reactions; Oxford University Press Inc.: New York, 1999
[3] Nicolau K.C., Snyder S.A., Montagnon T., Vassilikogiannakis G. Angew. Chem. Int. Ed. Engl., 2002, 41:1668
[4] Diels O., Alder K. Just. Liebigs Ann. Chem., 1928, 98:460
[5] Carruthers J.E., Carruthers W., Coldham I., Some Modern Methods of Organic Synthesis; Second ed.; Cambridge University Press, Cambridge, UK, 1978
[6] Carruthers W. Cycloadditions Reactions in Organic Synthesis; Pergamon, Oxford: UK, 1990; (b) Zare A., Mirzaei M., Rostami M., Jafari E. J. Med. Chem. Sci., 2020, 3:55; (c) Mirzaie A. J. Med. Chem. Sci., 2018, 1:31; (d) Nabati M., Bodaghi-Namileh V., Sarshar S. Prog. Chem. Biochem. Res., 2019, 2:108, doi: 10.33945/SAMI/PCBR.2019.2.4
[7] Geerlings P., Proft F.D., Langenaeker W. Chem. Rev., 2003, 103:1793
[8] Ess D.H., Jones G.O., Houk K.N. Adv. Synth. Catal., 2006, 348:2337
[9] Ormachea C.M., Mancini P.M.E., Kneeteman M.N., Domingo L.R. Computat. Theor. Chem., 2015, 1072:37
[10] Sarotti A.M. Org. Biomol. Chem., 2014, 12:187
[11] Mancinia P.M.E., Kneeteman M.N., Cainelli M., Ormachea C.M., Domingo L.R. J. Mol. Struct., 2017, 1147:155
[12] Breslow R., Maitra U., Rideout D. Tetrahedron Lett., 1983, 24:1901
[13] Cativiela C., Garcia J.I., Mayoral J.A., Avenoza A., Peregrina J.M., Roy M.A. J. Phys. Org. Chem., 1991, 4:48
[14] Cativiela C., García J.I., Mayoral J.A., Salvatella L. J. Chem. Soc. Perkin Trans., 1994, 847
[15] Ruiz-López M.F., Assfeld X., García J.I.X., Mayoral J.A., Salvatella L. J. Am. Chem. Soc., 1993, 115:8780
[16] Schneider H.J., Sangwan N.K. Angew. Chem. Int. Ed., 1987, 26:896
[17] Bini R., Chiappe C., Mestre V.L., Pomellic C.S., Welton T. Org. Biomol. Chem., 2008, 6:2522
[18] Chiappe C., Malvaldi M., Pomelli C.S. Green Chem., 2010, 12:1330
[19] Bini R., Chiappe C., Mestre V.L., Pomelli C.S., Welton T. Theor. Chem. Acc., 2009, 123:347
[20] Mancini P.M.E., Kneeteman M.N., Cainelli M., Ormachea C.M., Domingo L.R. J. Mol. Struct., 2017, 1147:155
[21] Ansari E.S., Ghiasi R., Forghaniha A. Struct. Chem., 2019, 30:30877
[22] Selvarengan P., Kolandaivel P. J. Mol. Struct. THEOCHEM, 2002, 617:99
[23] Allin S.B., Leslie T.M., Lumpkin R.S. Chem. Mater., 1996, 8:428
[24] Aquino A.J.A., Tunega D., Haberhauer G., Gerzabek M.H., Lischka H. J. Phys. Chem. A, 2002, 106:1862
[25] Springborg I.A.H.E.M. Specialist Periodical Reports: Chemical Modelling, Applications and Theory, vol. 5; Royal Society of Chemistry: Cambridge, UK, 2008
[26] Tomasi J., Mennucci B., Cammi R. Chem. Rev., 2005, 105:2999
[27] Rezazadeh M., Ghiasi R., Jamehbozorgi S. J. Struc. Chem., 2018, 59:245
[28] Ghiasi R., Zafarniya F., Ketabi S. Russian J. Inorg. Chem., 2017, 62:1371
[29] Alavi H., Ghiasi R. J. Struc. Chem., 2017, 58:30
[30] Zafarniya F., Ghiasi R., Jameh-Bozorghi S. Phys. Chem. Liq., 2017, 55:444
[31] Zafarnia F., Ghiasi R., Jamehbozorgi S. J. Struc. Chem., 2017, 58:1324
[32] Sadeghi N., Ghiasi R., Fazaeli R., Jamehbozorgi S. J. Appl. Spectros., 2016, 83:909
[33] Ghiasi R., Peikari A. Phys. Chem. Liq., 2017, 55:421
[34] Ghiasi R., Peikari A. Russian J. Phys. Chem. A, 2016, 90:2211
[35] Ghiasi R., Peikari A. J. Appl. Spectros., 2017, 84:148
[36] Ghiasi R., Pasdar H., Fereidoni S. Russian J. Inorg. Chem., 2016, 61:327
[37] Ghiasi R., Nemati M., Hakimioun A.H. J. Chil. Chem. Soc., 2016, 61:2921
[38] Peikari A., Ghiasi R., Pasdar H. Russian J. Phys. Chem. A., 2015, 89:250
[39] Ghiasi R., Amini E. J. Struct. Chem., 2015, 56:1483
[40] Fashami M.Z., Ghiasi R. J. Struct. Chem., 2015, 56:1474
[41] Rezazadeh M., Ghiasi R., Jamehbozorgi S. J. Appl. Spectros., 2018, 85:926
[42] Rezaeyani F., Ghiasi R., Yousefi M. Russian J. Phys. Chem. A, 2018, 92:1748
[43] Rahimi M., Ghiasi R. J. Mol. Liq., 2018, 265:164
[44] Ghiasi R. J. Mol. Liq., 2018, 264:616
[45] Nilchi M., Ghiasi R., Nasab E.M. J. Chilean. Chem. Soc., 2019, 64:4265
[46] Kazemi Z., Ghiasi R., Jamehbozorgi S. J. Struct. Chem., 2018, 59:1044
[47] Ghiasi R., Sadeghi N., Jamehbozorgi S. J. Struct. Chem., 2018, 59:1791
[48] Fereidoni S., Ghiasi R., Pasdar H. J. Struct. Chem., 2018, 59:1058
[49] Li D., Wanga Y., Han K. Coordinat. Chem. Rev., 2012, 256:1137
[50] Song G., Su Y., Periana R.A., Crabtree R.H., Han K., Zhang H., Li X. Angew. Chem. Int. Edit., 2010, 49:912
[51] Wang H., Wang Y., Han K.L., Peng X.J. J. Org. Chem., 2005, 70:4910
[52] Li D., Huang X., Han K., Zhan C.G. J. Am. Chem. Soc., 2011, 133:7416
[53] Ghiasi R., Fashami M.Z. J. Theor. Comput. Chem., 2014, 13:1450041
[54] Shajari N., Ghiasi R. J. Struc. Chem., 2018, 59:541
[55] Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., Scalman G., Barone V., Mennucci B., Petersson G.A., Nakatsuji H., Caricato M., Li X., Hratchian H.P., Izmaylov A.F., Bloino J., Zheng G., Sonnenberg J.L., Hada M., Ehara M., Toyota K., Fukuda R., Hasegawa J., Ishida M., Nakajima T., Honda Y., Kitao O., Nakai H., Vreven T., Montgomery J.A., Jr Peralta J.E., Ogliaro F., Bearpark M., Heyd J.J., Brothers E., Kudin K.N., Staroverov V.N., Kobayashi R., Normand J., Raghavachari K., Rendell A., Burant J.C., Iyengar S.S., Tomasi J., Cossi M., Rega N., Millam J.M., Klene M., Knox J.E., Cross J.B., Bakken V., Adamo C., Jaramillo J., Gomperts R., Stratmann R.E., Yazyev O., Austin A.J., Cammi R., Pomelli C., Ochterski J.W., Martin R.L., Morokuma K., Zakrzewski V.G., Voth G.A., Salvador P., Dannenberg J.J., Dapprich S., Daniels A.D., Farkas O., Foresman J.B., Ortiz J.V., Cioslowski J., Fox D.J. Gaussian 09. Revision A.02 ed.; Gaussian, Inc.: Wallingford CT, 2009.
[56] Hay P.J. J. Chem. Phys., 1977, 66:4377
[57] Krishnan R., Binkley J.S., Seeger R., Pople J.A. J. Chem. Phys., 1980, 72:650
[58] McLean A.D., Chandler G.S. J. Chem. Phys., 1980, 72:5639
[59] Wachters A.J.H. J. Chem. Phys., 1970, 52:1033
[60] Feller D. J. Comput. Chem., 1996, 17:1571
[61] Schuchardt K.L., Didier B.T., Elsethagen T., Sun L., Gurumoorthi V., Chase J., Li J., Windus T.L. J. Chem. Inf. Model, 2007, 47:1045
[62] Zhao Y., Truhla D.G. J. Phys. Chem. A, 2006, 110:5121
[63] Reed A.E., Curtiss L.A., Weinhold F. Chem. Rev., 1988, 88:899
[64] Glendening E.D., Reed A.E., Carpenter J.E., Weinhold F. NBO Version 3.1. Madison, 1988.
[65] Fukui K. Acc. Chem. Res., 1981, 14:363
[66] Fukui K. J. Phys. Chem., 1970, 74:4161
[67] Gonzalez C., Schlegel H.B., J. Phys. Chem., 1990, 94:5523
[68] Gonzalez C., Schlegel H.B. J. Chem. Phys., 1989, 90:2154
[69] Tomasi J., Mennucci B., Cammi R. Chem. Rev., 2005, 105:2999
[70] Domingo I.R. RSC Adv., 2014, 4:32415
[71] Jarmillo P., Domingo L.R., Chamorro E., Pe´rez P. J. Mol. Struct. (THEOCHEM), 2008, 865:68
[72] Wiberg K.B. Tetrahedron, 1968, 24:1083
[73] Moyano A., Perica`s M.A., Valenti E., J. Org. Chem., 1989, 54:573
[74] Manoharan M., Venuvanalingam P. J. Mol. Struct. (THEOCHEM), 1997, 394:41
[75] Manoharan M., Venuvanalingam P. J. Chem. Soc., Perkin Trans, 1997, 1799