آمار
| تعداد نشریات | 5 |
| تعداد شمارهها | 116 |
| تعداد مقالات | 1,333 |
| تعداد مشاهده مقاله | 1,336,430 |
| تعداد دریافت فایل اصل مقاله | 1,268,840 |
A Review on the Methods of Preparing 1,4-dihydropyridine derivatives | ||
| Communications In Catalysis | ||
| دوره 2، شماره 2، فروردین 2024، صفحه 56-84 اصل مقاله (1.2 M) | ||
| نوع مقاله: Review Article | ||
| شناسه دیجیتال (DOI): 10.22049/cic.2024.29549.1038 | ||
| نویسندگان | ||
| Adeleh Moshtaghi Zonouz؛ Saiedeh Abedinpour* | ||
| Department of Chemistry, Faculty of Basic Sciences, Azarbaijan Shahid Madani University, Tabriz, Iran | ||
| چکیده | ||
| Dihydropyridines are heterocyclic compounds that come in a variety of forms. It belongs to the hydrolyzed N-hetero-aromatic family of compounds. Numerous derivatives with different substituent, positioned at 2,6,3,5, and 1,4, are proven to occur and can be produced by cyclic synthesis, Hantzsch pyridine synthesis, decomposition type reaction. 1,4-DHP is a reliable agent for cure tuberculosis and it plays a key role in metabolic oxidation. They are a pharmacologically active substance and are regarded as a significant class of organic chemicals for their Ca chamber modular action. Marketed Drugs based on 1,4‐Dihydropyridine are used in the treatment of diseases such as cardiovascular Diseases, Infectious Diseases, Inflammatory diseases, Nervous diseases and Cancer. This review examines the types of these compounds that are used as drugs in the treatment of diseases and their synthesis methods. | ||
| کلیدواژهها | ||
| Dihydropyridines؛ 1؛ Synthesis of 1؛ 4‐Dihydropyridine | ||
| مراجع | ||
|
[1] Eisner, U.; Kuthan, J. Chem. Rev. 1972, 72, 1.
[2] Reddy, BP.; Rajesh, K.; Vijayakumar, V. Arab. J. Chem. 2015, 8, 138.
[3] Navidpour, L.; Shafaroodi, H.;, Miri, R.; Dehpour, A.R.; Shafiee, A. Il Farmaco. 2004, 59, 261.
[4] Triggle, D.J. Cell. Mol. Neurobiol. 2003, 23, 293.
[5] Budriesi, R.; Bisi, A.; Ioan, P.; Rampa, A.; Gobbi, S.; Belluti, F.; et al. Bioorg. Med. chem. 2005, 13, 3423.
[6] Maru, M.S.; Sudhadevi, Antharjanam, P.; Khan, NuH. ChemistrySelect. 2019, 4, 774.
[7] Bisi, A.; Micucci, M.; Gobbi, S.; Belluti, F.; Budriesi, R.; Rampa, A. Molecules. 2018, 23, 3088.
[8] Rasouli, Y.; Davood, A.; Alaee, A.; Dehqani, G.; Shafaroudi, H.; Lotfinia, M.; et al. Iran J Pharm Res. 2017, 16, 893.
[9] Prasanthi, G.; Prasad, K.; Bharathi, K. Eur. J. Med. Chem. 2014, 73, 97.
[10] Niemirowicz-Laskowska, K, Głuszek, K, Piktel, E.; Pajuste, K.; Durnaś, B.; Król, G, et al. Int J Nanomedicine. 2018, 13, 3411.
[11] Khedkar, S. A.; P. B.; Auti. Mini-Rev. Med. Chem. 2014, 14, 282.
[12] Fekri, L.Z. J. Chil. Chem. Soc. 2012, 57, 1415.
[13] Viradiya, D.; Mirza, S.; Shaikh, F.; Kakadiya, R.; Rathod, A.; Jain, N.; et al. Anticancer. Agents. Med. Chem. 2017, 17, 1003.
[14] Mollazadeh, S.; Shamsara, J.; Iman, M.; Hadizadeh, F. Recent. Pat. Anticancer. Drug. Discov. 2017, 12, 174.
[15] Iman, M.; Davood, A.; Lotfinia, M.; Dehqani, G.; Sardari, S.; Azerang, P.; et al. Iran J Pharm Res. 2016, 15, 791.
[16] Van Horn, K.S. 2013.
[17] Praveenkumar, E.; Gurrapu, N.; Kolluri, P.K.; Yerragunta, V.; Kunduru, B.R.; Subhashini, N. Bioorg Chem. 2019, 90, 103056.
[18] Edraki, N.; Mehdipour, A. R.; Khoshneviszadeh, M.; Miri, R. Drug Discov. Today. 2009, 14, 1058.
[19] Arrowsmith, J. E.; Campbell, S. F.; Cross, P. E.; Stubbs, J, K.; Burges, R. A.; Gardiner, D. G.; et al. J. Med. Chem. 1986, 29, 1696.
[20] Triggle, D. J. Drug Dev. Res. 2003, 58, 5.
[21] Vaghy, P. L.; Williams, J. S.; Schwartz, A. A.m J. Cardiol. 1987, 59, A9.
[22] Donald, P. R.; Van Helden, P. D. N. Engl. J. Med. 2009, 360, 2393.
[23] Tripathi, R. P.; Tewari, N.; Dwivedi, N.; Tiwari, V. K. Med. Res. Rev. 2005, 25, 93.
[24] Zhang, Y.; Post-Martens, K.; Denkin, S. Drug. Discov. Today. 2006, 11, 21.
[25] Trivedi, A. R.; Dodiya, D. K.; Dholariya, B. H.; Kataria, V. B.; Bhuva, V. R.; Shah, V. H. Bioorg. Med. Chem. Lett. 2011, 21, 5181.
[26] Khoshneviszadeh, M.; Edraki, N.; Javidnia, K.; Alborzi, A.; Pourabbas, B.; Mardaneh, J.; et al. Bioorg. Med. Chem. 2009, 17, 1579.
[27] Desai, B.; Sureja, D.; Naliapara, Y.; Shah, A.; Saxena, A. K. Bioorg. Med. Chem. 2001, 9, 1993.
[28] Kharkar, P. S.; Desai, B.; Gaveria, H.; Varu, B.; Loriya, R.; Naliapara, Y.; et al. J. Med. Chem. 2002, 45, 4858.
[29] Lentz, F.; Reiling, N.; Spengler, G.; Kincses, A.; Csonka, A.; Molnár, J.; et al. Molecules. 2019, 24, 2873.
[30] Murthy, Y.; Rajack, A.; Ramji, M. T.; Praveen, C.; Lakshmi, K. A. Bioorg. Med. Chem. Lett. 2012, 22, 6016.
[31] Lentz, F.; Hemmer, M.; Reiling, N.; Hilgeroth, A. Bioorg. Med. Chem. Lett. 2016, 26, 5896.
[32] Neubert, J. K.; Karai, L.; Jun, J. H.; Kim, H-S.; Olah, Z.; Iadarola, M. J. Pain. 2003, 104, 219.
[33] Karai, L.; Brown, D. C.; Mannes, A. J.; Connelly, S. T.; Brown, J.; Gandal, M.; et al. The Journal of clinical investigation. 2004, 113, 1344.
[34] Poondra, R. R.; Nallamelli, R. V.; Meda, C. L. T.; Srinivas, B.; Grover, A.; Muttabathula, J.; et al. Bioorg. Med. Chem. Lett. 2013, 23, 1104.
[35] Reddy, T. R.; Reddy, G. R.; Reddy, L. S.; Meda, C. L. T.; Parsa, K. V.; Kumar, K. S.; et al. Eur. J. Med. Chem. 2013, 62, 395.
[36] Revai, T.; Harmos, G. R. Soc. Med. 1999, 92, 23.
[37] Pedemonte, N.; Diena, T.; Caci, E.; Nieddu, E.; Mazzei, M.; Ravazzolo, R.; et al. Mol. Pharmacol. 2005, 68, 1736.
[38] Cateni, F.; Zacchigna, M.; Pedemonte, N.; Galietta, L. J.; Mazzei, M. T.; Fossa, P.; et al. Bioorg. Med. Chem. 2009, 17, 7894.
[39] Budriesi, R.; Ioan, P.; Leoni, A.; Pedemonte, N.; Locatelli, A.; Micucci , M.; et al. J. Med. Chem. 2011, 54, 3885.
[40] Kumar, A.; Singh, A. Pharmacol. Rep. 2015, 67, 195.
[41] Anand, R.; Gill, K. D.; Mahdi, A. A. Neuropharmacol. 2014, 76, 27.
[42] Gauthier, S.; Leuzy, A.; Racine, E.; Rosa-Neto, P. Prog. Neurobiol. 2013, 110, 102.
[43] Schelterns, P.; Feldman, H. The Lancet Neurol. 2003, 2, 539.
[44] Rosini, M.; Simoni, E.; Milelli, A.; Minarini, A.; Melchiorre, C. J. Med. Chem. 2013, 57, 2821.
[45] Bush, A. I. J. Alzheimer's Dis. 2008, 15, 223.
[46] Lahiri, D.; Rogers, J.; Greig, N.; Sambamurti, K. Curr. Pharm. Des. 2004, 10, 3111.
[47] Wilkinson, D.; Wirth, Y.; Goebel, C. Dement. Geriatr. Cogn. Disord. 2014, 37, 71.
[48] León, R.; de los Ríos, C.; Marco-Contelles, J.; Huertas, O.; Barril, X.; Luque, F. J.; et al. Bioorg. Med. Chem. 2008, 16, 7759.
[49] Alptüzün, V.; Prinz, M.; Hörr, V.; Scheiber, J.; Radacki, K.; Fallarero, A.; et al. Bioorg. Med. Chem. 2010, 18, 2049.
[50] Tenti, G.; Egea, J.; Villarroya, M.; León, R.; Fernández, J. C.; Padín, J. F.; et al. Med.Chem. Comm. 2013, 4, 90.
[51] Malek, R.; Maj, M.; Wnorowski, A.; Jóźwiak, K.; Martin, H.; Iriepa, I.; et al. Bioorg. Chem. 2019, 103205.
[52] Teodori, E.; Dei, S.; Scapecchi, S.; Gualtieri, F. Il Farmaco. 2002, 57, 385.
[53] Szabo, D.; Keyzer, H.; Kaiser, H. E.; Molnar, J. Anticancer Res. 2000, 20, 4261.
[54] Dantzig, A.; Law, K.; Cao, J.; Starling, J. Curr. Med. Chem. 2001, 8, 39.
[55] Colabufo, A. N.; Berardi, F.; Grazia Perrone, M.; Capparelli, E.; Cantore, M.; Inglese, C.; et al. Curr. Top. Med. Chem. 2010, 10, 1703.
[56] Baumert, C.; Hilgeroth, A. (Formerly Current Medicinal Chemistry-Anti-Cancer Agents). 2009, 9, 415.
[57] Ranjbar, S.; Firuzi, O.; Edraki, N.; Shahraki, O.; Saso, L.; Khoshneviszadeh, M.; et al. Med. Chem. Comm. 2017, 8, 1919.
[58] Kawase, M.; Shah, A.; Gaveriya, H.; Motohashi, N.; Sakagami, H.; Varga, A.; et al. Bioorg. Med. Chem. 2002, 10, 1051.
[59] Baumert, C.; Günthel, M.; Krawczyk, S.; Hemmer, M.; Wersig, T.; Langner, A.; et al. Bioorg. Med. Chem. 20132, 1, 166.
[60] Sirisha, K.; Shekhar, M. C.; Umasankar, K.; Mahendar, P.; Sadanandam, A.; Achaiah, G.; et al. Bioorg. Med. Chem. 2011, 19, 3249.
[61] Coburger, C.; Wollmann, J.; Krug, M.; Baumert, C.; Seifert, M.; Molnár, J.; et al. Bioorg. Med. Chem. 2010, 18, 4983.
[62] Voigt, B.; Coburger, C.; Monár, J.; Hilgeroth, A. Bioorg. Med. Chem. 2007, 15, 5110.
[63] Nejati, M.; Sadeghpour, H.; Ranjbar, S.; Javidnia, K.; Edraki, N.; Saso, L.; et al. Can. J. Chem. 2019, 1.
[64] Goto, R. N.; Sobral, L. M.; Sousa, L. O.; Garcia, C. B.; Lopes, N. P.; Marín-Prida, J.; et al. Eur. J. Pharmacol. 2018, 819, 198.
[65] Hantzsch, A. Justus Liebigs Ann. Chem. 1882, 215, 1.
[66] Breitenbucher, J. G.; Figliozzi, G. Tetrahedron Lett. 2000, 41, 4311.
[67] Sapkal, S. B.; Shelke, K. F.; Shingate, B. B.; Shingare, M. S. Tetrahedron Lett. 2009, 50, 1754.
[68] Correa, W. H.; Scott, J. L. Green Chem. 2001, 3, 296.
[69] Ghosh, P. P.; Paul, S.; Das A. R. Tetrahedron Lett. 2013, 54, 138.
[70] Baraldi, P. T.; Noel, T.; Wang, Q.; Hessel ,V. Tetrahedron Lett. 2014, 55, 2090.
[71] Khodja, I. A.; Ghalem, W.; Dehimat, Z. I.; Boulcina, R.; Carboni, B.; Debache, A. Synth. Commun. 2014, 44, 959.
[72] Ma, X.; He, Y.; Lu, M. Synth. Commun. 2014, 44, 474.
[73] Patil, R. D.; Dalal, S. D. Lett. Org. Chem. 2011, 8, 477.
[74] Lee, J. H. Tetrahedron Lett. 2005, 46, 7329.
[75] Akbari, J.; Tala, S.; Dhaduk, M.; Joshi, H. Arkivoc. 2008, 12, 126.
[76] Yadav, J.; Reddy, B.; Basak, A.; Narsaiah, A. Green chem. 2003, 5, 60.
[77] Auria-Luna, F.; Marqués-López, E.; Herrera, P. R. Molecules. 2018, 23, 2692.
[78] Kolvari, E.; Zolfigol, M.; Koukabi, N.; Shirmardi-Shaghasemi, B. Chem. Pap. 2011, 65, 898.
[79] Makone, S.; Niwadange, S. Chem Sin. 2012, 3, 1293.
[80] Wang, S-X.; Li, Z-Y.; Zhang, J-C.; Li, J-T. Ultrason. Sonochem. 2008, 15, 677.
[81] Zonouz, A. M.; Sahranavard, N. J. Chem. 2010, 7, S372.
[82] Marques, M. V.; Ruthner, M. M.; Fontoura, L. A.; Russowsky, D. J. Braz. Chem. Soc. 2012, 23, 171.
[83] Yang, J.; Jiang, C.; Yang, J.; Qian, C.; Fang, D. Green chem. lett. rev. 2013, 6, 262.
[84] Hajinasiri, R.; Rezayati, S. Z. fur Naturforsch. 2013, 68, 818.
[85] Shaabani, A.; Maleki, A.; Rezayan, A. H.; Sarvary, A. Mol. Divers. 2011, 15, 41.
[86] Balme, G.; Bossharth, E.; Monteiro, N. Eur. J. Org. Chem. 2003, 2003, 4101.
[87] Polshettiwar, V.; Varma, R. S. Green Chem. 2010, 12, 743.
[88] Kumar, A.; Maurya, R. A. Synlett. 2008, 2008, 883.
[89] Cherkupally, S. R.; Mekala, R.. Chem. Pharm. Bull. 2008, 56, 1002.
[90] Giorgi, G.; Adamo, M. F.; Ponticelli, F.; Ventura, A. Org. Biomol. Chem. 2010, 8, 5339.
[91] Demirci, T.; Çelik, B.; Yıldız, Y.; Eriş, S.; Arslan, M.; Sen, F.; et al. RSC Adv. 2016, 6, 76948.
[92] Tabrizian, E.; Amoozadeh, A. RSC Adv. 2016, 6, 96606.
[93] Chen, W.; Peng, X-w.; Zhong, L-x.; Li, Y.; Sun, R-c. ACS Sustain. Chem. Eng. 2015, 3, 1366.
[94] Moghaddam, F. M.; Saberi, V.; Keshavarz, S. SynOpen. 2018, 2, 0036.
[95] Zhang, M.; Liu, Y-H.; Shang, Z-R.; Hu, H-C.; Zhang, Z-H. Comm. 2017, 88, 39.
[96] Mirjalili, B. B. F.; Bamoniri, A.; Asadollah Salmanpoor, L. J Nanostruct. 2018, 8, 276.
[97] Chughtai, A. H.; Ahmad, N.; Younus, H. A.; Laypkov, A.; Verpoort, F. Chem. Soc. Rev. 2015, 44, 6804.
[98] Devarajan, N.; Karthik, M.; Suresh, P. Org. Biomol. Chem. 2017, 15, 9191.
[99] Jiang, J.; Yaghi, O. M. Chem. Rev. 2015, 115, 6966.
[100] Lin, Y.; Kong, C.; Chen, L. RSC Adv. 2016, 6, 32598.
[101] Devarajan, N.; Suresh, P. New J Chem. 2019, 43, 6806.
[102] Arzehgar, Z.; Sajjadifar, S.; Arandiyan, H. Asian J. Green Chem.2019, 3, 43.
[103] Nasr-Esfahani, M.; Hoseini, S. J.; Montazerozohori, M.; Mehrabi, R.; Nasrabadi, H. J. Mol. Catal. A Chem. 2014, 382, 99.
[104] Mahinpour, R.; Moradi, L.; Zahraei, Z.; Pahlevanzadeh, N. J. Saudi Chem. Soc. 2018, 22, 876.
[105] Liu, Y-p.; Liu, J-m.; Wang, X.; Cheng, T-m.; Li, R-t. Tetrahedron. 2013, 69, 5242.
[106] Zonouz, A. M.; Aras, M. A.; Abuali, N. Transit. Met. Chem. 2013, 38, 335.
[107] Zonouz, A. M.; Hosseini S. B. Synth. Commun. 2008, 38, 290.
[108] Rao, G. D.; Nagakalyan, S.; Prasad, G. RSC Adv. 2017, 7, 3611.
[109] Tajbakhsh, M.; Alinezhad, H.; Norouzi, M.; Baghery, S.; Akbari, M. J. Mol. Liq. 2013, 177, 44.
[110] Otokesh, S.; Koukabi, N.; Kolvari, E.; Amoozadeh, A.; Malmir, M.; Azhari, S. S. Afr. j. chem. 2015, 68, 15.
[111] Davoodnia, A.; Khashi, M.; Tavakoli-Hoseini, N. Chinese. J. Catal. 2013, 34, 1173.
[112] Masoudi, P. J. Sci. I. R. Iran. 2019, 30, 33.
[113] Khaskel, A.; Barman, P. Heteroat. Chem. 2016, 27, 114.
[114] Ghasemzadeh, M. A.; Nasrollahi, S. M. H.; Zolfaghari, M. R. Acta Chim. Slov. 2018, 65, 199.
[115] Mirzaei, H.; Davoodnia, A. Chinese. J. Catal. 2012, 33, 1502.
[116] Vahdat, S. M.; Chekin, F.; Hatami, M.; Khavarpour, M.; Baghery, S.; Roshan-Kouhi, Z. Chinese. J. Catal. 2013, 34, 758.
[117] Liu, P.; Hao, J-W.; Mo, L-P.; Zhang, Z-H. RSC Adv. 2015, 5, 48675.
[118] Irimia-Vladu, M. Chem. Soc. Rev. 2014, 43, 588.
[119] Dallinger, D.; Kappe, C. O. Chem. Rev. 2007, 107, 2563.
[120] Chanda, A.; Fokin, V. V. Chem. Rev. 2009, 109, 725.
[121] Lindström, U. M. Chem. Rev. 2002, 102, 2751.
[122] Wang, Z-X.; Qin, H-L. Green Chem. 2004, 6, 90.
[123] Moshtaghi Zonouz, A.; Raeisolsadati Oskouei, M. J. Chin. Chem. Soc. 2013, 60, 275.
[124] Tamaddon, F.; Razmi, Z.; Jafari, A. A. Tetrahedron Lett. 2010, 51, 1187.
[125] Sharma, V. K.; Singh, S. K. RSC Adv. 2017, 7, 2682.
[126] Ostaszewski, R.; Paprocki, D.; Madej, A.; Koszelewski, D.; Brodzka, A. Front. Chem. 2018, 6, 502.
[127] Sharma, M.; Rajani, D.; Patel, H. Royal Society open science. 2017, 4, 170006.
[128] Pramanik, A.; Saha, M.; Bhar, S. ISRN Org. Chem. 2012, 2012.
[129] Longo, Jr L. S.; Craveiro, M. V. J. Braz. Chem. Soc. 2018, 29, 1999.
[130] Constable, D. J.; Jimenez-Gonzalez, C.; Henderson, R. K. Org. Process Res. Dev. 2007, 11, 133.
[131] Alfonsi, K.; Colberg, J.; Dunn, P. J.; Fevig, T.; Jennings, S.; Johnson, T. A.; et al. Green Chem. 2008, 10, 31.
[132] Henderson, R. K.; Jiménez-González, C.; Constable, D. J.; Alston, S. R.; Inglis, G. G.; Fisher, G.; et al. Green Chem. 2011, 13, 854.
[133] Prat, D.; Pardigon, O.; Flemming, H-W.; Letestu, S.; Ducandas, Vr.; Isnard, P.; et al. Org. Process Res. Dev. 2013, 17, 1517.
[134] Hallett, J. P.; Welton, T. Chem. Rev. 2011, 111, 3508.
[135] Olivier-Bourbigou, H.; Magna, L.; Morvan, D. Appl. Catal. A Gen. 2010, 373, 1.
[136] Wasserscheid, P.; Welton, T. John Wiley & Sons; 2008.
[137] Deetlefs, M.; Seddon, K. R. Green Chemistry. 2010, 12, 17.
[138] Rogers, R. D.; Seddon, K. R. Sci. 2003, 302, 792.
[139] Ghandi, K. Curr. Opin. Green Sustain. Chem. 2014, 4, 44.
[140] Cole, A. C.; Jensen, J. L.; Ntai, I.; Tran, K. L. T.; Weaver, K. J.; Forbes, D. C.; et al. J. Am. Chem. Soc. 2002, 124, 5962.
[141] Isambert, N.; Duque, Md. M. S.; Plaquevent, J-C.; Genisson, Y.; Rodriguez, J.; Constantieux, T. Chem. Soc. Rev. 2011, 40, 1347.
[142] Liu, X.; Liu, B. J. Chem. 2017, 2017.
[143] Rostamnia, S.; Hassankhani, A. Synlett. 2014, 25, 2753.
[144] Abaszadeh, M.; Seifi, M. J. Sulphur Chem. 2017, 38, 440.
[145] Sajjadifar, S.; Mohammadi-Aghdam, S. Asian J. Green Chem. 2017, 1, 1.
[146] Liu, T.; Lai, Y-H.; Yu, Y-Q.; Xu, D-Z. New J Chem. 2018, 42, 1046.
[147] Gericke, M.; Fardim, P.; Heinze, T. Molecules. 2012, 17, 7458.
[148] Perozo, E.; Rees, D.C. Curr. Opin. Struct. Biol. 2003, 13, 432.
[149] Rani, M.; Brant, A.; Crowhurst, L.; Dolan, A.; Lui, M.; Hassan, N. H.; et al. Phys. Chem. Chem. 2011, 13, 16831.
[150] Abbott, A. P.; Capper, G.; Davies, D. L.; Rasheed, R. K.; Tambyrajah, V. Chem. Commun. 2003, 70.
[151] Imperato, G.; Eibler, E.; Niedermaier, J.; König, B. Chem. Commun. 2005, 1170.
[152] Imperato, G.; Höger, S.; Lenoir, D.; König, B. Green Chem. 2006, 8, 1051.
[153] Francisco, M.; van den Bruinhorst, A.; Kroon, M. C. Angew. Chem., Int. Ed. Engl. 2013, 52, 3074.
[154] Dai, Y.; van Spronsen, J.; Witkamp, G-J.; Verpoorte, R.; Choi, YH. Anal. Chim. Acta. 2013, 766, 61.
[155] Skopek, M. A.; Mohamoud, M. A.; Ryde,r K. S.; Hillman, A. R. Chem. Commun. 2009, 935.
[156] Carriazo, D.; Serrano, M. C.; Gutiérrez, M. C.; Ferrer, M. L.; del Monte, F. Chem. Soc. Rev. 2012, 41, 4996.
[157] Zhao, H.; Baker, G. A. J. Chem. Technol. Biotechnol. 2013, 88, 3.
[158] Del Monte, F.; Carriazo, D.; Serrano, M. C.; Gutierrez, M. C.; Ferrer, M. L. ChemSusChem. 2014, 7, 999.
[159] Rodríguez, N. R.; González, A. S.; Tijssen, P. M.; Kroon, M. C. Fluid Ph. Equilibria. 2015, 385, 72.
[160] Abo-Hamad, A.; Hayyan, M.; AlSaadi, M. A.; Hashim, M. A. J. Chem. Eng. 2015, 273, 551.
[161] Pednekar, S.; Bhalerao, R.; Ghadge, N. Chem. Sci. J. 2013, 125, 615.
[162] Wang, L.; Zhu, K-Q.; Chen, Q.; He, M-Y. Green Process. Synth. 2014, 3, 457.
[163] Kumar, J. A.; Shridhar, G.; Ladage, S.; Ravishankar, L. Synth. Commun. 2016, 46, 1989.
[164] Cravotto, G.; Cintas, P. Chem. Soc. Rev. 2006, 35, 180.
[165] Xu, H.; Zeiger, B. W.; Suslick, K. S. Chem. Soc. Rev. 2013, 42, 2555.
[166] Puri, S.; Kaur, B.; Parmar, A.; Kumar, H. Curr. Org. Chem. 2013, 17, 1790.
[167] Pourian, E.; Javanshir, S.; Dolatkhah, Z.; Molaei, S.; Maleki, A. ACS Omega. 2018, 3, 5012.
[168] Kulkarni, P. J. Chil. Chem. Soc. 2014, 59, 2319.
[169] Tekale, S. U.; Pagore, V. P.; Kauthale, S. S.; Pawar, R. P. Chin. Chem. Lett. 2014, 25, 1149.
[170] Yoo, J. S.; Laughlin, T. J.; Krob, J. J.; Mohan, R. S. Tetrahedron Lett. 2015, 56, 4060.
[171] Moradi, L.; Zare, M. Green chem. lett. rev. 2018, 11, 197.
[172] Tabassum, S.; Govindaraju, S.; Pasha, M. RSC Adv. 2016, 6, 29802.
[173] Ozer, E. K.; Gunduz, M. G.; El-Khouly, A.; Sara, Y.; Simsek, R.; Iskit, A. B.; et al. Turk. J. Biochem. 2018, 43, 578.
[174] Abaszadeh, M.; Seifi, M.; Asadipour, A. Res. Chem. Intermed. 2015, 41, 5229.
[175] Zonouz, A. M.; Eskandari, I.; Khavasi, H. R. Tetrahedron Lett. 2012, 53, 5519.
[176] Leonardi, M.; Villacampa, M.; Menéndez, J. C. Chem. Sci. 2018, 9, 2042.
[177] Hernandez, J. G.; Bolm, C. J. Org. Chem. 2017, 82, 4007.
[178] Kumar, S.; Sharma, P.; Kapoor, K. K.; Hundal, M. S. Tetrahedron. 2008, 64, 536.
[179] Ghahremanzadeh, R.; Ahadi, S.; Shakibaei, G. I.; Bazgir, A. Tetrahedron Lett. 2010, 51, 499.
[180] Kumar, A.; Sharma, S. Green Chem. 2011, 13, 2017.
[181] Jiang, L.; Ye, L. D.; Gu, J.; Su, W. k.; Ye, W. t. J. Chem. Technol. Biotechnol. 2019, 94, 2555.
[182] Moshtaghi, Z. A.; Okhravi, S.; Moghani, D. Monatsh. Chem. 2016, 147, 1819.
[183] Zeng, J-C.; Yu, F.; Asiri, A. M.; Marwani, H. M.; Zhang, Z. J. Rev. Comm. Heterocycle. Chem. 2017, 94, 2054.
[184] Moshtaghi, Z. A.; Oskuie, M. R.; Mollazadeh, S. Synth. Commun. 2005, 35, 2895.
[185] Moshtaghi, Z. A.; Sadr, M. H.; Oskuie, M. R.; Bachechi, F. J. Chin. Chem. Soc. 2010, 57, 1081.
[186] Rastgar Mirzaei, Y.; Moshtaghi Zonouz, A. Iran. J. Chem. Chem. Eng. 1997, 16, 29.
[187] Moshtaghi, Z.; Raisossadat, O.; Sadeghi, S. Q. Arkivoc. 2006, 15.
[188] Auria-Luna, F.; Marqués-López, E.; Mohammadi, S.; Heiran, R.; Herrera, R. Molecules. 2015, 20, 15807.
[189] Auria-Luna, F.; Marqués-López, E.; Gimeno, M. Cn.; Heiran, R.; Mohammadi, S.; Herrera, R. P. J. Org. Chem. 2017, 82, 5516.
[190] Lamm, B.; Simonsson, R.; Sundell, S. Tetrahedron Lett. 1989, 30, 6423.
[191] Yamamoto, T.; Ohno, S.; Niwa, S.; Tokumasu, M.; Hagihara, M.; Koganei, H, et al. Bioorg. Med. Chem. Lett. 2011, 21, 3317.
[192] Jiang, J.; Yu, J.; Sun, X. X.; Rao, Q. Q.; Gong, L. Z. Angew. Chem. Int. Ed. 2008, 47, 2458.
[193] He, W.; Shi, X.; Huan, M; Huang, Q-j.; Zhou, S-y. Bioorg. Med. Chem. Lett. 2010, 20, 805.
[194] Gotrane, D. M.; Deshmukh, R. D.; Ranade, P. V.; Sonawane, S. P.; Bhawal, B. M.; Gharpure, M. M.; et al. Org. Process Res. Dev. 2010, 14, 640.
| ||
|
آمار تعداد مشاهده مقاله: 1,443 تعداد دریافت فایل اصل مقاله: 641 |
||