References
- M.T. Maghsoodlou, R. Heydari, S.M. Habibi-Khorassani, N. Hazeri, M. Lashkari, M. Rostamizadeh, and S.S. Sajadikhah, Synth. Commun. 41, 569–578 (2011). doi:https://doi.org/10.1080/00397911003629432.
- a) W.J. Ross, W.B. Jamieson, and M.C. Mccowen, J. Med. Chem. 16, 347–352 (1973). doi:https://doi.org/10.1021/jm00262a008;b) 1 A.F. Cockerill, D.M. Rackham, and N.C. Franklin, J. Chem. Soc. Perkin Trans. 2, 509 (1973). doi:https://doi.org/10.1039/p29730000509; c) 1 C. Yang, L. Lee, and Y. Wang, J. Chinese Chem. Soc. 50, 445 (2003). doi:https://doi.org/10.1002/jccs.200300-070; d) I. Row, Y. Liu, and C. Whang, J. Chinese Chem. Soc. 37, 203 (1990). doi:https://doi.org/10.1002/jccs.199000028; e) C. Chen, P. Lin, and N. Hsieh, J. Chinese Chem. Soc. 16, 37 (1969). doi:https://doi.org/10.1002/jccs.196900008.
- a) F.S. Julian, J. Chem. Soc. Perkin Trans. 1, 3119 (1994). doi:https://doi.org/10.1039/P19940003119; b) A.E. Feiring and E.R. Wonchoba, J. Org. Chem. 57, 7014 (1992). doi:https://doi.org/10.1021/jo00052a008; c) J.G. Buchanan and H.Z. Sable, in Selective Organic Transformations, edited by B.S. Thyagarajan (Wiley-Interscience, New York, 1972) Vol. 2, pp. 1.
- a) S.J. Barker and R.C. Storr, J. Chem. Soc. Perkin Trans. 1, 485 (1990). doi:https://doi.org/10.1039/p19900000485; b) A. Maquestiau, D. Beugnies, R. Flammang, A.R. Katritzky, M. Soleiman, T. Davis, and J.N. Lam, J. Chem. Soc. Perkin Trans. 2, 1071 (1988). doi:https://doi.org/10.1039/p29880001071; c) P.A. Wender and C.B. Cooper, Tetrahedron. 42, 2985 (1986). doi:https://doi.org/10.1016/S0040-4020(01)90589-7.
- C.G. Fortuna, V. Barresi, G. Berellini, and G. Musumarra, Bioorg. Med. Chem. 16, 4150–4159 (2008). doi:https://doi.org/10.1016/j.bmc.2007.12.042.
- P. Martins, J. Jesus, S. Santos, L.R. Raposo, C. Roma-rodrigues, P.V. Baptista, and A.R. Fernandes, Molecules 20, 16852 (2015). doi:https://doi.org/10.3390/molecules200916852.
- K.-S. Huang, C.-H. Yang, S.-L. Huang, C.-Y. Chen, Y.-Y. Lu, and Y.-S. Lin, Int. J. Mol. Sci. 17, 1578 (2016). doi:https://doi.org/10.3390/ijms17091578.
- T. Esatbeyoglu, K. Ulbrich, C. Rehberg, S. Rohn, and G. Rimbach, Food Funct. 6, 887–893 (2015). doi:https://doi.org/10.1039/C4FO00790E.
- A.K. Gupta, S. Madan, D.K. Majumdar, and A. Maitra, Int. J. Pharm. 209, 1–14 (2000). doi:https://doi.org/10.1016/S0378-5173(00)-00508-1.
- J.J. Li, Name Reactions (Springer, New York, 2003).
- R.S. Bahare, S. Ganguly, K. Choowongkomon, and S. Seetaha, DARU J. Pharm. Sci. 23, 6 (2015). doi:https://doi.org/10.1186/s40-199-014-0086-1.
- N. Trotsko, U. Kosikowska, A. Paneth, T. Plech, A. Malm, and M. Wujec, Molecules. 23, 1023 (2018). doi:https://doi.org/10.3390/molecules23051023.
- A.R. Boobis, A.M. Lynch, S. Murray, R. de la Torre, A. Solans, M. Farre, J. Segura, N.J. Gooderham, and D.S. Davies, Cancer Res. 54, 89 (1994. doi:https://doi.org/10.1002/central/CN-00097718/full#0.
- A.F. Pozharskii, A.T. Soldatenkov, and A.R. Katritzky, Heterocycles in Life and Society: An Introduction to Heterocyclic Chemistry, Biochemistry and Applications, 2nd ed. (John Wiley & Sons, 2011). doi: https://doi.org/10.1002/9781119998372.
- M.M. Heravi and T. Alishiri. Dimethyl Acetylenedicarboxylate as a Building Block in Heterocyclic Synthesis. in Advances in Heterocyclic Chemistry (Elsevier, 2014), 113, pp. 1–66. doi:https://doi.org/10.1016/B978-0-12-800170-7.00001-8.
- C.E. Quinn, P.K. Hamilton, C.J. Lockhart, and G.E. McVeigh, Br. J. Pharmacol. 153, 636–645 (2008). doi:https://doi.org/10.1038/sj.bjp.0707452.
- R.E. Soccio, E.R. Chen, and M.A. Lazar, Cell Metab. 20, 573–591 (2014). doi:https://doi.org/10.1016/j.cmet.2014.08.005.
- N.C. Desai, U.P. Pandit, and A. Dodiya, Expert Opin. Ther. Pat. 25, 479–488 (2015). doi:https://doi.org/10.1517/13543776.2014.1001738.
- M.J. Naim, M.J. Alam, S. Ahmad, F. Nawaz, N. Shrivastava, M. Sahu, and O. Alam, Eur. J. Med. Chem. 129, 218–250 (2017). doi:https://doi.org/10.1016/j.ejmech.2017.02.031.
- D. Rudavath, R. Sreenivasulu, S.R. Pinapati, and R.R. Raju, Asian J. Chem. 30, 1201–1204 (2018). doi:https://doi.org/10.14233/ajchem.2018.21114.
- N. Abdul-kader Saleh, H. El-abd Saltani, F. Abbas Al-Issa, Abul-kasem E.A., and A.-S. Gomaa Melad, J. Chinese Chem. Soc. 60, 1234–1358 (2013). doi:https://doi.org/10.1002/jccs.2013-00048.
- F. Ghodsi, M. Shahraki, S.M. Habibi-Khorassani, and M. Shokoohian, Phosphorus. Sulfur. Silicon Relat. Elem. 192, 929–935 (2017). doi:https://doi.org/10.1080/10426507.2017.1292274.
- F. Ghodsi, S.M. Habibi-Khorassani, and M. Shahraki, Molecules. 21, 1 (2016). doi:https://doi.org/10.3390/molecules21111514.
- S.M. Habibi-Khorassani, A. Ebrahimi, M. Maghsoodlou, O. Asheri, M. Shahraki, N. Akbarzadeh, and Y. Ghalandarzehi, Int. J. Chem. Kinet. 45, 596–612 (2013). doi:https://doi.org/10.1002/kin.20797.
- O. Asheri, S.M. Habibi-Khorassani, and M. Shahraki, Prog. React. Kinet. Mech. 43, 286–299 (2018). doi:https://doi.org/10.3184/146867818X15319903829218.
- a) S. Talaiefar, S.M. Habibi-Khorassani, and M. Shaharaki, Polycycl. Aromat. Compd. 1 (2020). doi:https://doi.org/10.1080/10406-638.2020.1751667; b) S. Talaiefar, S.M. Habibi-Khorassani, M. Sharaki, and E. Mollashahi, Polycycl. Aromat. Compd. 0, 1 (2019) ; c) S.M. Habibi-Khorassani, M.T. Maghsoodlou, M. Shahraki, S. Talaiefar, M.A.Kazemian, and J. Aboonajmi, Res. Chem. Intermed. 41, 5821 (2015). doi:https://doi.org/10.1007/s11164-014-1704-8; d) S.M. Habibi-Khorassani, M.T. Maghsoodlou, S. Talaiefar, M.A. Kazemian, and J. Aboonajmi, Lett. Org. Chem. 11, 413 (2014). doi:https://doi.org/10.2174/15701786113106660086; b) S. Talaiefar, S.M. Habibi-Khorassani, M. Sharaki, and E. Mollashahi, Polycycl. Aromat. Compd. 41, 143 (2021). doi:https://doi.org/10.1080/10406638.2019.1570953; c) S.M. Habibi-Khorassani, M.T. Maghsoodlou, M. Shahraki, S. Talaiefar, M.A. Kazemian, and J. Aboonajmi, Res. Chem. Intermed. 41, 5821 (2015). doi:https://doi.org/10.1007/s11164-014-1704-8; d) S.M. Habibi-Khorassani, M.T. Maghsoodlou, S. Talaiefar, M.A. Kazemian, and J. Aboonajmi, Lett. Org. Chem. 11, 413 (2014). doi:https://doi.org/10.2174/15701786113106660086; e) S.M. Habibi-Khorassani, M. Shahraki, and S. Talaiefar, Phosphorus, Sulfur Silicon Relat. Elem. 196, 300 (2020). doi:https://doi.org/10.1080/10426507.2020.1833330; f) O. Asheri, M. Shahraki, and S.M. Habibi-Khorassani, Polycycl. Aromat. Compd. 40, 714 (2018). doi:https://doi.org/10.1080/10406638.2018.1481109.
- a) M. Darijani, S.M. Habibi-Khorassani, and M. Shahraki, Prog. React. Kinet. Mech. 43, 79–90 (2018). doi:https://doi.org/10.3184/146867818X15161889114439; b) S.M. Habibi-Khorassani, M. Shahraki, and M. Darijani, Chem. Cent. J. 11, 71 (2017). doi:https://doi.org/10.1186/s13065-017-0297-x.
- S.S. Pawar, U. Phalgune, and A. Kumar, J. Org. Chem. 64, 7055 (1999). doi:https://doi.org/10.1021/jo990583z.
- J. Benitez, M. del Mar Graciani, C.D. Hubbard, and F. Sanchez-Burgos, J. Solution Chem. 19, 19–29 (1990). doi:https://doi.org/10.1007/BF00650641.
- a) J.T. Carstensen, J. Pharm. Sci. 59, 1140–1143 (1970). doi:https://doi.org/10.1002/jps.2600590817; b) S. Lin and J. Jwo, J. Chinese Chem. Soc. 35, 85 (1988). doi:https://doi.org/10.1002/jccs.198800-013.
- J.N. Bronsted, Chem. Rev. 5, 231–338 (1928). doi:https://doi.org/10.1021/cr60019a001.
- R. Saeed, S.R. Khan, and M. Ashfaq, Asian J. Chem. 24 (8), 3745–3750 (2012).
- T. Vilariño, P. Alonso, X.L. Armesto, P. Rodríguez, and M.E. De Sastre Vicente, J. Chem. Res. Part S. 9,, 558-559 (1998). doi:https://doi.org/10.1039/a801853g.
- L.M. Schwartz and R.I. Gelb, Anal. Chem. 50, 1592–1594 (1978). doi:https://doi.org/10.1021/ac50033a055.
- H. Ys, G. Mckay, H. Ys, and G. Mckay, Process Biochem. 34, 451–465 (1999). doi:https://doi.org/10.1016/S0032-9592(98)00112-5.
- K.C. Huang, R.A. Couttenye, and G.E. Hoag, Chemosphere. 49, 413–420 (2002). doi:https://doi.org/10.1016/S0045-6535(02)-00330-2.
- S.M. Habibi-Khorassani, M. Shahraki, and B. Mostafa, Mini. Rev. Org. Chem. 16, 59–77 (2019). doi:https://doi.org/10.2174/1570193X15666180612085855.
- S.M. Habibi-Khorassani, M. Shahraki, and M. Dehdab, ChemistrySelect. 1, 6069–6078 (2016). doi:https://doi.org/10.1002/slct.201600435.
- G. Lente, I. Fábián, and A. J. Poë, and New J. Chem 29, 759 (2005). doi:https://doi.org/10.1039/b501687h.
- P.A. Tregloan and G.S. Laurence, J. Sci. Instrum. 42, 869–872 (1965). doi:https://doi.org/10.1088/0950-7671/42/12/310.
- M. Castaneda-Agullo, L.M. Del Castillo, J.R. Whitaker, and A.L. Tappel, J. Gen. Physiol. 44, 1103–1120 (1961). doi:https://doi.org/10.1085/jgp.44.6.1103.
- D.S. Mahadevappa, K.S. Rangappa, N.M.M. Gowda, and B.T. Gowda, J. Phys. Chem. 85, 3651–3658 (1981). doi:https://doi.org/10.1021/j150624a025.
- C.A. Ward, J. Chem. Phys. 79, 5605–5615 (1983). doi:https://doi.org/10.1063/1.445681.
- V. Holba, Chem. Pap. 28, 17 (1974).
- P. Muller, Pure Appl. Chem. 66, 1077–1184 (1994). doi:https://doi.org/10.1351/pac199466051077.
- M. Rachwalska, I. Natkaniec, Z.H. Urbanek, and D. Majda, Zeitschrift Für Phys. Chemie. 226, 291–314 (2012). doi:https://doi.org/10.1524/zpch.2012.0189.
- M.A. Wolff, Instrum. Sci. Technol. 5, 59 (1974). doi:https://doi.org/10.1080/10739147408543357.
- C. Lee, W. Yang, and R.G. Parr, Phys. Rev. B. 37, 785–789 (1988). doi:https://doi.org/10.1103/PhysRevB.37.785.
- O.I. Osman, Mol. Phys. 112, 304–315 (2014). doi:https://doi.org/10.1080/00268976.2013.810310.
- A. Buczek and M.A. Broda, Mol. Phys. 112, 639–644 (2014). doi:https://doi.org/10.1080/00268976.2013.847979.
- M. De La Pierre, M. Bruno, C. Manfredotti, F. Nestola, M. Prencipe, and C. Manfredotti, Mol. Phys. 112, 1030–1039 (2014). doi:https://doi.org/10.1080/00268976.2013.829250.
- a) J.S. Wright, C.N. Rowley, and L.L. Chepelev, Mol. Phys. 103, 815–823 (2005). doi:https://doi.org/10.1080/00268970412331333-429; b) C.F. Wilcox and S.H. Bauer, Mol. Phys. 103, 2829 (2005). doi:https://doi.org/10.1080/00268970500093902; c) J.P. Finley, Mol. Phys. 102, 627 (2004). doi:https://doi.org/10.1080/0026897041000-1687452.
- S.M. Habibi-Khorassani, M. Shahraki, and H. Yaghoubian, J. Chinese Chem. Soc. 64, 195–204 (2017). doi:https://doi.org/10.1002/jccs.201600765.
- L.R. Domingo, M.J. Aurell, R. Jalal, and M. Esseffar, Comput. Theor. Chem. 986, 6–13 (2012). doi:https://doi.org/10.1016/j.comp-tc.2012.01.035.
- a) L.R. Domingo, M. Ríos-Gutiérrez, and S. Emamian, RSC Adv. 7, 15586–15595 (2017). doi:https://doi.org/10.1039/C7RA005-44J; b) F. Ghodsi, M. Shahraki, S.M. Habibi-Khorassani, M. Nassiri, and M. Fazilatkhah, Polycycl. Aromat. Compd. 40, 840 (2020). doi:https://doi.org/10.1080/10406638.2018.1485714.
- H.B. Schlegel, J. Comput. Chem. 3, 214–218 (1982). doi:https://doi.org/10.1002/jcc.540030212.
- J. Tomasi and M. Persico, Chem. Rev. 94, 2027–2094 (1994). doi:https://doi.org/10.1021/cr00031a013.
- V. Barone, M. Cossi, and J. Tomasi, J. Comput. Chem. 19, 404–417 (1998). doi:https://doi.org/10.1002/(SICI)1096-987X(199803)-19:4<404::AID-JCC3>3.0.CO;2-W.
- L.R. Domingo, M. Ríos-Gutiérrez, and P. Pérez, Tetrahedron. 72, 1524–1532 (2016). doi:https://doi.org/10.1016/j.tet.2016.01.061.
- M. Frisch, G. Trucks, H. Schlegel, G. Scuseria, M. Robb, J. Cheeseman, and G. Scalmani, Revis. A. 3, 310 (2016).
- J.W. Furness, U. Ekström, T. Helgaker, and A.M. Teale, Mol. Phys. 114, 1415–1422 (2016). doi:https://doi.org/10.1080/00268976.2015.1133859.
- A.D. Becke and K.E. Edgecombe, J. Chem. Phys. 92, 5397–5403 (1990). doi:https://doi.org/10.1063/1.458517.
- S. Noury, X. Krokidis, F. Fuster, and B. Silvi, Comput. Chem. 23, 597–604 (1999). doi:https://doi.org/10.1016/S0097-8485(99)-00039-X.
- R.G. Parr and R.G. Pearson, J. Am. Chem. Soc. 105, 7512–7516 (1983). doi:https://doi.org/10.1021/ja00364a005.
- R.G. Parr, L. v Szentpály, and S. Liu, J. Am. Chem. Soc. 121, 1922–1924 (1999). doi:https://doi.org/10.1021/ja983494x.
- L.R. Domingo, E. Chamorro, and P. Pérez, J. Org. Chem. 73, 4615–4624 (2008). doi:https://doi.org/10.1021/jo800572a.
- W. Kohn and L.J. Sham, Phys. Rev. 140, A1133–A1138 (1965). doi:https://doi.org/10.1103/PhysRev.140.A1133.
- P. Jaramillo, L.R. Domingo, E. Chamorro, and P. Pérez, J. Mol. Struct. Theochem. 865, 68–72 (2008). doi:https://doi.org/10.1016/j.theochem.2008.06.022.
- B. Silvi, J. Mol. Struct. 614, 3–10 (2002). doi:https://doi.org/10.1016/S0022-2860(02)00231-4.