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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 50, 2020 - Issue 20
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Synthetic Communications Reviews

A review: Recent progress on the synthetic routes to 1(5)-substituted 1H-Tetrazoles and its analogs

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Pages 3017-3043 | Received 23 Jun 2020, Published online: 15 Jul 2020

References

  • Herr, R. J. Bioorg. Med. Chem. 2002, 10, 3379–3393. DOI: 10.1016/S0968-0896(02)00239-0.
  • Hochegger, P.; Faist, J.; Seebacher, W.; Saf, R.; Maser, P.; Kaiser, M.; Weis, R. Med. Chem. 2019, 15, 409–416. DOI: 10.2174/1573406414666181015115101.
  • Malik, M. A.; Al-Thabaiti, S. A.; Malik, M. A. Int. J. Mol. Sci. 2012, 13, 10880–10898. DOI: 10.3390/ijms130910880.
  • Vembu, S.; Parasuraman, P.; Gopalakrishnan, M. J. Pharm. Res. 2014, 8, 1552.
  • Vembu, S.; Parasuraman, P.; Gopalakrishnan, M. Der. Pharma. Chemica. 2014, 6, 35.
  • Varadaraji, D.; Suban, S. S.; Ramasamy, V. R.; Kubendiran, K.; Raguraman, J. S. K.; Nalilu, S. K.; Pati, H. N. Org. Commun. 2010, 3, 45.
  • Ramakrishna, V.; Sai, L.; Ravindranath, L. K. Med. Chem. 2017, 7, 239.
  • Mohite, P. B.; Pandhare, R. B.; Khanage, S. G. Analele Unive. Din Bucuresti 2011, 20, 107.
  • Lamie, P. F.; Philoppes, J. N.; Azouz, A. A.; Safwat, N. M. J. Enzyme Inhib. Med. Chem. 2017, 32, 805–820. DOI: 10.1080/14756366.2017.1326110.
  • Singh, S. Lett. Drug Des. Disc. 2009, 6, 286–297. DOI: 10.2174/157018009788452483.
  • Popova, E. A.; Protas, A. V.; Trifonov, R. E. Anticancer Agents Med. Chem. 2017, 17, 1856.
  • Moderhack, D. J. Prakt. Chem. 1998, 340, 687–709. DOI: 10.1002/prac.19983400802.
  • Boteju, L. W.; Hruby, V. J. Tetrahedron Lett. 1993, 34, 1757–1760. DOI: 10.1016/S0040-4039(00)60771-2.
  • Vembu, S.; Pazhamalai, S.; Gopalakrishnan, M. Med. Chem. Res. 2016, 25, 1916–1924. DOI: 10.1007/s00044-016-1627-6.
  • Naeimi, H.; Kiani, F.; Moradian, M. Iranian J. Catal. 2013, 3, 243.
  • Habibi, D.; Nabavi, H.; Nasrollahzadeh, M. J. Chem. 2013, 2013, 1–4. DOI: 10.1155/2013/645313.
  • Naeimi, H.; Kiani, F.; Moradian, M. J. Nanopart. Res. 2014, 16, 2590. ‏ DOI: 10.1007/s11051-014-2590-0.
  • Naeimi, H.; Kiani, F. Ultrason. Sonochem. 2015, 27, 408–415. DOI: 10.1016/j.ultsonch.2015.06.008.
  • Rostami-Vartooni, A.; Alizadeh, M.; Bagherzadeh, M. Beilstein J. Nanotechnol. 2015, 6, 2300–2309. DOI: 10.3762/bjnano.6.236.
  • Habibi, D.; Pakravan, N.; Arabi, A.; Kaboudvand, Z. Appl. Organometal. Chem. 2018, 32(1), e3988.‏1. DOI: 10.1002/aoc.3988.
  • Habibi, D.; Heydari, S.; Gil, A.; Afsharfarnia, M.; Faraji, A.; Karamian, R.; Asadbegy, M. Appl.Organomet. Chem. 2018, 32, e4005.‏1.
  • Habibi, D.; Nasrollahzadeh, M.; Mehrabi, L.; Mostafaee, S. Monatsh. Chem. 2013, 144, 725–728. DOI: 10.1007/s00706-012-0871-9.
  • Habibi, D.; Mostafaee, S.; Mehrabi, L. J. Chem. Res. 2013, 37, 464–466. DOI: 10.3184/174751913X13729393880865.
  • Potewar, T. M.; Siddiqui, S. A.; Lahoti, R. J.; Srinivasan, K. V. Tetrahedron Lett. 2007, 48, 1721–1724. DOI: 10.1016/j.tetlet.2007.01.050.
  • Wang, H.; Wei, F.; Chen, Q.; Hu, X.; Niu, X. J. Chem. Res. 2016, 40, 570–572. DOI: 10.3184/174751916X14721249985304.
  • Habibi, D.; Nasrollahzadeh, M.; Kamali, T. A. Green Chem. 2011, 13, 3499. DOI: 10.1039/c1gc15245a.
  • Dehghani, F.; Sardarian, A. R.; Esmaeilpour, M. J. Organomet. Chem. 2013, 743, 87–96. DOI: 10.1016/j.jorganchem.2013.06.019.
  • Esmaeilpour, M.; Javidi, J.; Zahmatkesh, S. Appl. Organometal. Chem. 2016, 30, 897–904. DOI: 10.1002/aoc.3518.
  • Esmaeilpour, M.; Javidi, J.; Dodeji, F. N.; Abarghoui, M. M. J. Mol. Catal. A: Chem. 2014, 393, 18–29. DOI: 10.1016/j.molcata.2014.06.001.
  • Sharghi, H.; Ebrahimpourmoghaddam, S.; Doroodmand, M. M. J. Organomet. Chem. 2013, 738, 41–48. DOI: 10.1016/j.jorganchem.2013.04.013.
  • Khalafi-Nezhad, A.; Mohammadi, S. RSC Adv. 2013, 3, 4362. DOI: 10.1039/c3ra23107k.
  • Sajadi, S. M.; Maham, M. Lett. Org. Chem. 2014, 11, 35–39. DOI: 10.2174/157017861101140113160634.
  • Sheridan, U.; Gallagher, J. F.; Bjerrum, M. J.; Fleming, A.; Kelleher, F.; McGinley, J. Inorg. Chim. Acta 2014, 421, 200–209. DOI: 10.1016/j.ica.2014.05.028.
  • Finnegan, W. G.; Henry, R. A.; Lofquist, R. J. Am. Chem. Soc. 1958, 80, 3908–3911. DOI: 10.1021/ja01548a028.
  • Tao, C.; Wang, B.; Sun, L.; Yi, J.; Shi, D.; Wang, J.; Liu, W. J. Chem. Res. 2017, 41, 25–29. DOI: 10.3184/174751917X14815427219248.
  • Shie, J. J.; Fang, J. M. J. Org. Chem. 2007, 72, 3141–3144. DOI: 10.1021/jo0625352.
  • Zhao, B.; Ren, Y. L.; Ren, F.; Tian, X.; Zhao, S. Lett. Org. Chem. 2018, 15, 627–632. DOI: 10.2174/1570178615666180213094610.
  • Demko, Z. P.; Sharpless, K. B. J. Org. Chem. 2001, 66, 7945–7950. DOI: 10.1021/jo010635w.
  • Chauvière, G.; Bouteille, B.; Enanga, B.; de Albuquerque, C.; Croft, S. L.; Dumas, M.; Périé, J. J. Med. Chem. 2003, 46, 427–440. DOI: 10.1021/jm021030a.
  • Ansari, K. F.; Lal, C. Eur. J. Med. Chem. 2009, 44, 4028–4033. DOI: 10.1016/j.ejmech.2009.04.037.
  • Dofe, V. S.; Sarkate, A. P.; Kathwate, S. H.; Gill, C. H. Heterocycl. Commun. 2017, 23, 325.
  • Gowd, M. R. M. B.; Pasha, M. A. J. Chem. Soc. 2011, 123, 75.
  • Akhlaghinia, B.; Rezazadeh, S. J. Braz. Chem. Soc. 2012, 23, 2197–2203. DOI: 10.1590/S0103-50532013005000005.
  • Zamani, L.; Mirjalili, B. B. F.; Zomorodian, K.; Zomorodian, S. S. Afr. J. Chem. 2015, 68, 133.
  • AuCreggi, V.; Franckevičius, V.; Kitching, M. O.; Ley, S. V.; Longbottom, D. A.; Oelke, A. J.; Sedelmeier, G. Org. Synth. 2008, 85, 72-87. DOI: 10.1002/0471264229.os085.09.
  • Najafi, P.; Modarresi-Alam, A. R. Res. J. Chem. Env. Sci. 2013, 1, 28.
  • Dhayanithi, V.; Shafi, S. S.; Kumaran, K.; Jai, S. K.; Ragavan, V. R.; Goud, K. S. P.; Kumari, N. S.; Pati, H. N. J. Serb. Chem. Soc. 2011, 76, 165–175. DOI: 10.2298/JSC090421001D.
  • Karimi Zarchi, M. A.; Nazem, F. J. Appl. Polym. Sci. 2012, 123, 1977–1982. DOI: 10.1002/app.34701.
  • Zarchi, M. A. K.; Nazem, F. J. Iran. Chem. Soc. 2014, 11, 91–99. DOI: 10.1007/s13738-013-0279-4.
  • Nishiyama, K.; Watanabe, A. Chem. Lett. 1984, 13, 455–458. DOI: 10.1246/cl.1984.455.
  • Aridoss, G.; Laali, K. K. Eur. J. Org. Chem. 2011, 2011, 2827–2835. DOI: 10.1002/ejoc.201100128.
  • Luo, K.; Meng, L.; Zhang, Y.; Zhang, X.; Wang, L. Adv. Synth. Catal. 2013, 355, 765–780. DOI: 10.1002/adsc.201200868.
  • Bernhart, C. A.; Perreaut, P. M.; Ferrari, B. P.; Muneaux, Y. A.; Assens, J. L.; Clement, J.; Haudricourt, F.; Muneaux, C. F.; Taillades, J. E.; Vignal, M. A. J. Med. Chem. 1993, 36, 3371–3380. DOI: 10.1021/jm00074a018.
  • Rao, S. N.; Babu, K. S. Org. Commun. 2011, 4, 105.
  • Himasekar, C.; Mustafa, S.; Babu, M. S. Open Chem. J. 2019, 6, 1–7. DOI: 10.2174/1874842201906010001.
  • Dorababu, A.; Kamble, R. R.; Kattimani, P. P. Lett. Org. Chem. 2013, 10, 510–517. DOI: 10.2174/1570178611310070009.

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