[1] M.L. Barreca, A. Rao, L. De Luca, M. Zappala, C. Gurnari, P. Monforte, E. De Clercq, B.V. Maele, Z. Debyser, M. Witvrouw, J.M. Briggs, A. Chimirri, J. Chem. Inform. Comput. Sci., 2004, 44, 1450–1455.
[2] K. Pandya, P.S. Desai, World J. Pharm. Res., 2018, 7, 465-474.
[3] N. Kolocouris, A. Kolocouris, G.B. Foscolos, G. Fytas, J. Neyts, E. Padalko, J. Balzarini, R. Snoeck, G. Andrei, E. De Clercq. J. Med. Chem., 1996, 39, 3307–3318.
[4] K.M. Pandya, P.S. Desai, N.B. Patel, B.P. Dave, Chem. Biol. Interface, 2018, 8, 314-322
[5] V.O. Koz’minykh, N.M. Igidov, S.S. Zykova, V.E. Kolla, N.S. Shuklina, T. Odegova, Pharm. Chem. J., 2002, 36, 188–191
[6] K.M. Pandya, Synthesis and Cytotoxicity of Azaheterocyclic Compounds. Thesis, Rowan University: New Jersey, 2018.
[7] T.A. Silina, V.L. Gein, L.F. Gein, E.V. Voronina, Pharm. Chem. J., 2003, 37, 585–587.
[8] V.L. Gein, E.V. Voronina, T.E. Ryumina, G.N. Novoselova, K.D. Potemkin, Y.S. Andreichikov, Pharm. Chem. J., 1996, 30, 25–26.
[9] F. Lovren, I.D. Gaon, B. Bobarevic, Arch. Pharm., 1990, 323, 901–904.
[10] T. Sano, Y. Horiguchi, J. Toda, K. Imafuku, Y. Tsuda, Chem. Pharm. Bull., 1984, 32, 497–503.
[11] A.J. Aasen, C.C. Culvenor, J. Org. Chem., 1969, 34, 4143– 4147.
[12] B.M. Goldschmidt, Substituted pyrrolizidines, J. Org. Chem., 1962, 27, 4057–4058.
[13] J.J. Tufariello, J.P. Tette, J. Org. Chem., 1975, 40, 3866–3869.
[14] K. M. Pandya, A.H. Patel, P.S.Desai, Chem Afr., 2019. https://doi.org/10.1007/s42250-019-00096-5
[15] C.J.H. Morton, R. Gilmour, D.M. Smith, P. Lightfoot, A.M.Z. Slawin, E. MacLean, Tetrahedron, 2002, 58, 5547–5565.
[16] A. Ueda, Y. Sekiya, M. Taniguchi, Japanese Patent JP 2,003,165,918, 2003.
[17] K. Pandya, R. Patel, J. Chem. Chem. Sci., 2017, 7, 1331-1341.
[18] J.M. Adam, P.V. Dalvi, V.S. Ekkundi, J.P. Bacher, S. Tiwari, World Patent WO 2,004,083,170, 2004.
[19] J.M. Adam, P.V. Dalvi, V.S. Ekkundi, J.P. Bacher, R. Sreenivasan, D.M. Rane, World Patent WO 2,004,089,941, 2004.
[20] H. Shiraishi, T. Nishitani, S. Sakaguchi, Y. Ishii, J. Org. Chem., 1998, 63, 6234–6238.
[21] X. Lin, Z. Mao, X. Dai, P. Lu, Y. Wang, Chem. Commun., 2011, 47, 6620–6622.
[22] O.A. Attanasi, G. Favi, F. Mantellini, G. Moscatelli, S. Santeusanio, J. Org. Chem. 2011, 76, 2860–2866.
[23] E. Ghabraie, S. Balalaie, M. Bararjanian, H.R. Bijanzadeh, F. Rominger, Tetrahedron, 2011, 67, 5415–5420.
[24] C.R. Reddy, M.D. Reddy, B. Srikanth, K.R. Prasad, Org. Biomol. Chem., 2011, 9, 6027–6033.
[25] B.M. Trost, J.-P. Lumb, J.M. Azzarelli, J. Am. Chem. Soc., 2011, 133, 740–743.
[26] A.V. Gulevich, A.S. Dudnik, N. Chernyak, V. Gevorgyan, Chem. Rev., 2013, 113, 3084–3213.
[27] H.C. Brown, U.R. Khire, G. Narla, U.S. Racherla, J. Org. Chem., 1995, 60, 544–549.
[28] O. Yuryeva, Y. Kondratova, L. Logoyda, Asian J. Pharm. Clin. Res., 2018, 11, 200–204.
[29] A.R. Karimi, Z. Alimohammadia, J. Azizian, A.A. Mohammadi, M.R. Mohammadi-Zadeh, Catal. Commun., 2006, 7, 728–732.
[30] A.O. Eseola, W. Li, W.H. Sun, M. Zhang, L. Xiao, J. A. Woods, Dyes Pigments, 2011, 88, 262–273.
[31] R. Hosseinnia, M. Mamaghani, K. Tabatabaeian, F. Shirini, M. Rassa, Bioorg. Med. Chem. Lett., 2012, 22, 5956–5960.
[32] B. Yilmaz, U. Kocak, J. Adv. Pharm. Res., 2019, 3, 17–22.
[33] D.A. Dougherty, Acc. Chem. Res., 2013, 46, 885-893.
[34] R. Leon, A.G. Garcia, J. Marco-Contelles, Med. Res. Rev., 2013, 33, 139.
[35] M. Metwally, M. Gouda, A.N. Harmal, A. Khalil, Eur. J. Med. Chem., 2012, 56, 254–262.
[36] H.P. Shah, B.R. Shah, J.J. Bhatt, N.C. Desai, P.B. Trivedi, N.K. Undavia, Indian. J. Chem. B, 1998, 37, 180-182.
[37] S.M. El-Khawas, N.S. Habib, J. Hetero. Chem., 1989, 26, 177–181.
[38] R.R. Somani, P.Y. Shirodkar, V.J. Kadam, Chin. J. Chem., 2008, 26, 117-1731.
[39] D.K. Shukla, S.D. Srivastava, Indian J. Chem., 2008, 47, 463-469.
[40] M. Tabcheh, M. Baroudi, F. El-omar, A. Elzant, M. Elkhatib, V. Rolland, Asian J. Chem., 2006, 18, 1771–1782.
[41] S.B. Rose, R.B. Miller, J. Bacteriol., 1939, 38, 525-537.
[42] C.A. Lipinski, F. Lombardo, B.W. Dominy, P.J. Feeney, Adv. Drug Deliv. Rev., 2001, 46, 3–26.