[1] Kozma D., Acs M., Fogassy E., Tetrahedron, 1994, 50:6907
[2] Fogassy E., Nógrádi M., Pálovics E., Schindler J., Synthesis, 2005, 10:1568
[3] Storey R. A., Ymen I., Solid State Characterization of Pharmaceuticals, John Wiley & Sons, 2011
[4] Vasileiadis M., Pantelides C. C., Adjiman C. S., Chem. Eng. Sci., 2015, 121:60
[5] Nangia A., Acc. Chem. Res., 2008, 41:595.
[6] Matsuura T., Koshima H., J. Photochem. Photobiol., 2005, 6:7
[7] Brock C.P., Schweizer W.B., Dunitz J.D., J. Am. Chem. Soc., 1991, 113:9811
[8] Fuhrhop J.H., Schnieder P., Rosenberg J., Boekema E., J. Am. Chem. Soc., 1987, 109:3387
[9] Jacques J., Collet A., Wilen S.H., Collet A., Enantiomers, racemates, and resolutions, Wiley New York, 1981
[10] Ziegler M., Davis A.V., Johnson D.W., Raymond K.N., Angew. Chem. Int. Ed., 2003, 42:665
[11] Biswas A., Estarellas C., Frontera A., Ballester P., Drew M.G., Gamez P., A. Ghosh P., Cryst. Eng. Comm., 2012, 14:5854
[12] König W.A., Icheln D., Runge T., Pfaffenberger B., Ludwig P., Hühnerfuss H., J. High Resolut. Chromatogr., 1991, 14:530
[13] Armstrong D.W., Chang C.D., Li W.Y., J. Agric. Food Chem., 1990, 38:1674
[14] Hoekstra P.F., Hara T.M., Karlsson H., Solomon K.R., Muir D.C., Environ. Toxicol. Chem., 2003, 22:2482
[15] Solano D.M., Hoyos P., Hernáiz M., Alcántara A., Sánchez-Montero J., Bioresour. Technol., 2012, 115:196
[16] Ranjan P., Pandey A., Binod P., J. Basic Microbiol., 2017, 57:762
[17] Eriksson T., Bjöurkman S., Roth B., Fyge Å., Höuglund P., Chirality, 1995, 7:44
[18] Testa B., Trager W.F., Chirality, 1990, 2:29
[19] Katrusiak A., Katrusiak A., J. Pharm. Sci., 2004, 93:3066
[20] Cai W., Marciniak J.d., Andrzejewski M., Katrusiak A., J. Phys. Chem. C, 2013, 117:7279
[21] Mori K., Chirality, 2011, 23:449
[22] Kinbara K., Synlett, 2005, 5:0732
[23] Leusen F.J., Cryst. Growth Des., 2003, 3:189
[24] Gavezzotti A., Rizzato S., J. Org. Chem. 2014, 79: 4809.
[25] M. Leclercq J. Jacques, Brienne M.-J., Tetrahedron, 1981, 37:1727
[26] Choubdari E., Fakhraian H., Peyrovi M. H., Tetrahedron: Asymmetry, 2013, 24:801
[27] Choubdari E., Fakhraian H., Peyrovi M. H., Chirality, 2014, 26:183
[28] Fakhraian H., Toulabi H., Choubdari E., Peyrovi M. H., Haj Ghanbary H., Org. Prep. Proced. INT., 2015, 47:141
[29] Salimi M., Zarenezhad B., Fakhraian H., Choobdari E., J. Appl. Solution Chem. Model., 2015, 4:143
[30] Fakhraiana H., Salimi M., Zarenezhad B., Choobdari E., Phys. Chem. Res., 2016, 4:663
[31] Zarei V., Javadi N., Ghahramani Z., Fakhraian H., J. Sci. Islam. Repub. Iran, 2019, 30:241
[32] Cullen L., Br. Vet. J., 1996, 152:519
[33] Virtanen R., Savola J.-M., Saano V., Nyman L., Eur. J. Pharmacol., 1988, 150:9
[34] Kuusela E., Raekallio M., Anttila M., Falck I., Mölsä S., Vainio O., J. Vet. Pharmacol. Ther., 2000, 23:15
[35] Savola J.-M., Virtanen R., Eur. J. Pharmacol., 1991, 195:193
[36] Bhana N., Goa K.L., McClellan K.J., Drugs, 2000, 59:263
[37] Krait S., Salgado A., Chankvetadze B., Gago F., Scriba G.K., J. Chromatogr. A, 2018, 1567:198
[38] Scott-Warren V., Sebastian J., Bja Educ., 2015, 16:242
[39] Bennett R.C., Restitutti F., Companion Animal, 2016, 21:128
[40] Kaboudin B., Haghighat H., Aieni S., Behrouzi L., Kazemi F., Kato J.-Y., Aoyama H., Yokomatsu T., J. Iran. Chem. Soc., 2017, 14:1735
[41] Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., Montgomery J.A., Vreven T., Kudin K.N., Burant J.C., Millam J.M., Iyengar S.S., Tomasi J., Barone V., Mennucci B., Cossi M., Scalmani G., Rega N., Petersson G.A., Nakatsuji H., Hada M., Ehara M., Toyota K., Fukuda R., Hasegawa J., Ishida M., Nakajima T., Honda Y., Kitao O., Nakai H., Klene M., Li X., Knox J.E., Hratchian H.P., 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., Ayala P.Y., Morokuma K., Voth G.A., Salvador P., Dannenberg J.J., Zakrzewski V.G., Dapprich S., Daniels A.D., Strain M.C., Farkas O., Malick D.K., Rabuck A.D., Raghavachari K., Foresman J.B., Ortiz J.V., Cui Q., Baboul A.G., Clifford S., Cioslowski J., Stefanov B.B., Liu G., Liashenko A., Piskorz P., Komaromi I., Martin R.L., Fox D.J., Keith T., Laham A., Peng C.Y., Nanayakkara A., Challacombe M., Gill P.M.W., Johnson B., Chen W., Wong M.W., Gonzalez C., Pople J.A., Gaussian 03, Revision B.03, Gaussian, Inc., Pittsburgh PA, 2003
[42] Discover Accelrys, Materials Studio 3.0, San Diego, CA, 2004
[43] Bader R.F.W., Atoms in Molecules, Oxford University Press, UK, 1990
[44] Keith T.A., AIMAll (Version 10.07. 25), Overland Park, KS, USA: TK Gristmill Software, 2010