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A Brief Review on Schiff Base, Synthesis, and Their Antimicrobial Activities

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Abstract

The Schiff base chemsitry includes compounds that attracted the attention of research scope from the early years. Consequently, the Schiff base constitutes a significant source of compounds for new pharmacological developments. Several Schiff bases, including derivatives, were synthesized and assessed for biological activities they possess, containing antimicrobial, antioxidant, anti-inflammatory, anti-tuberculosis, anticonvulsants, anxiolytics, antidepressant, anticancer, antihypertensive,and anti-fungal activity. The Schiff Base research, including composites with a lower-side effect, and extra specific activity and remains a dynamic zone of debate in medicinal chemistry. The current wrok elaborately discusses the medicinal chemistry and its bio-logical qualities.

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DATA AVAILABILITY

The data that support the findings of this study are available from the corresponding author upon reasonable request.

REFERENCES

  1. Da Silva,C.M., da Silva D.L., Modolo, L.V., Alves, R.B., de Resende, M.A., Martins, C.V., and de Fátima, Â., J. Adv. Res., 2011,vol. 2, pp. 1–8. https://doi.org/10.1016/j.jare.2010.05.004

  2. Dhar, D.N. and Taploo, C., J. Sci. Ind. Res., 1982, vol. 41, pp. 501­–506.

    CAS  Google Scholar 

  3. Li, S., Chen, S., Lei, S., Ma, H., Yu, R., and Liu, D., Corros. Sci., 1999, vol. 41, pp. 1273–1287. https://doi.org/10.1016/S0010-938X(98)00183-8

    Article  CAS  Google Scholar 

  4. Aboul-Fadl, T., Mohammed, F.A.H., and Hassan, E.A.S., Arch. Pharm. Res., 2003, vol. 26, pp. 778–784. https://doi.org/10.1007/BF02980020

    Article  CAS  PubMed  Google Scholar 

  5. Sondhi, S.M., Singh, N., Kumar, A., Lozach, O., and Meijer, L., Bioorg. Med. Chem., 2006, vol. 14, pp. 3758–3765. https://doi.org/10.1016/j.bmc.2006.01.054

    Article  CAS  PubMed  Google Scholar 

  6. Avaji, P.G., Kumar, C.V., Patil, S.A., Shivananda, K., and Nagaraju, C., Eur. J. Med. Chem., 2009, vol. 44, pp. 3552­–3559. https://doi.org/10.1016/j.ejmech.2009.03.032

    Article  CAS  PubMed  Google Scholar 

  7. Przybylski, P., Huczynski, A., Pyta, K., Brzezinski, B., and Bartl, F., Curr. Org. Chem., 2009, vol. 13, pp. 124–148. https://doi.org/10.2174/138527209787193774

    Article  CAS  Google Scholar 

  8. Chinnasamy, R.P., Sundararajan, R., and Govindaraj, S., J. Adv. Pham. Technol., 2010, vol. 1, p. 342. https://doi.org/10.4103/0110-5558.72428

    Article  CAS  Google Scholar 

  9. Mounika, K., Pragathi, A., and Gyanakumari, C., J. Sci. Res., 2010, vol. 2, p. 513. https://doi.org/10.3329/jsr.v2i3.4899

    Article  CAS  Google Scholar 

  10. Venkatesh, P., Asian J. Pharm. Heal. Sci., 2011, vol. 1, pp. 8–11. https://ajphs.com/article/2011/1/1/8-11s

    Google Scholar 

  11. Chaubey, A. and Pandeya, S., Int. J. Pharm. Res., 2012, vol. 4, pp. 590–598. https://www.sphinxsai.com

    CAS  Google Scholar 

  12. Udupi, R., J. Chem. Pharm. Res., 2012, vol. 4, pp. 1151–1159. https://www.jocpr.com/articles/synthesis-and-biological-screening-of-certain-new-triazole-schiff-bases-and-their-derivatives-bearing-substituted-benzot.pdf

    Google Scholar 

  13. Bringmann, G., Dreyer, M., Faber, J.H., Dalsgaard, P.W., Stærk, D., Jaroszewski, J.W., and Christensen, S.B., J. Nat. Prod., 2004, vol. 67, pp. 743–748. https://pubs.acs.org/doi/abs/10.1021/np0340549

    Article  CAS  PubMed  Google Scholar 

  14. Guo, Z., Xing, R., Liu, S., Zhong, Z., Ji, X., Wang, L., and Li, P., Carbohydr. Res., 2007, vol. 342, pp. 1329–1332. https://doi.org/10.1016/j.carres.2007.04.006

    Article  CAS  PubMed  Google Scholar 

  15. Souza, A.O.D., Galetti, F., Silva, C.L., Bicalho, B., Parma, M.M., Fonseca, S.F., and Bezerra, F., Quím. Nova, 2007, vol. 30, pp. 1563–1566. https://doi.org/10.1590/S0100-40422007000700012

    Article  Google Scholar 

  16. Imrie, C., Kleyi, P., Nyamori, V.O., Gerber, T.I., Levendis, D.C, and Look, J., J. Organomet. Chem., 2007, vol. 692, pp. 3443–3453. https://doi.org/10.1016/j.jorganchem.2007.04.011s

    Article  CAS  Google Scholar 

  17. Verma, M., Pandeya, S.N., Singh, K.N., and Stables, J.P., Acta Pharm., 2004, vol. 54, pp. 49–56. https://hrcak.srce.hr/16661

    CAS  PubMed  Google Scholar 

  18. Gupta, J., De, B., and Saravanan, V., Indian J. Chem., 2006, vol. 45B, pp. 2580–2582. https://rb.gy/uzsxd8

    Google Scholar 

  19. Cates, L.A. and Rashed, M.S., Pharm. Res., 1984, vol. 1, pp. 271–274. https://link.springer.com/article/10.1023/A:1016350119870

    Article  CAS  PubMed  Google Scholar 

  20. Kayser, O., Kiderlen, A., and Croft, S., Parasitol. Res., 2003, vol. 90, pp. S55–S62. https://doi.org/10.1007/s00436-002-0768-3

  21. Chohan, Z.H., Praveen, M., and Ghaffar, A., J. Met. Drugs, 1997, vol. 4, pp. 267–272. https://downloads.hindawi.com/archive/1997/803138.pdf

    CAS  Google Scholar 

  22. Ershad, S., Sagathforoush, L., Karim-Nezhad, G., and Kangari, S., Int. J. Electrochem. Sci., 2009, vol. 4, pp. 846–854. https://rb.gy/uzsxd8

    Article  CAS  Google Scholar 

  23. Tisato, F., Refosco, F., and Bandoli, G., Coord. Chem. Rev., 1994, vol. 135, pp. 325–397. https://doi.org/10.1016/0010-8545(94)80072-3

    Article  Google Scholar 

  24. Jarrahpour, A., Khalili, D., De Clercq, E., Salmi, C., and Brunel, J.M., Molecules, 2007, vol. 12, pp. 1720–1730. https://doi.org/10.3390/12081720

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Bhattacharya, A., Purohit, V.C., and Rinaldi, F., Org. Process Res. Dev., 2003, vol. 7, pp. 254–258. https://pubs.acs.org/doi/abs/10.1021/op020222c

    Article  CAS  Google Scholar 

  26. Sundriyal, S., Sharma, R.K., and Jain, R., Curr. Med. Chem., 2006, vol. 13, pp. 1321–1335. https://doi.org/10.2174/092986706776873023

    Article  CAS  PubMed  Google Scholar 

  27. Nucci, M. and Marr, K.A., Clin. Infect. Dis., 2005, vol. 41, pp. 521–526. https://doi.org/10.1086/432060

    Article  PubMed  Google Scholar 

  28. Martins, C., Da Silva, D., Neres, A., Magalhaes, T., Watanabe, G., Modolo, L., and De Resende, M., J. Antimicrob. Chemother., 2009, vol. 63, pp. 337–339. https://doi.org/10.1093/jac/dkn488

    Article  CAS  PubMed  Google Scholar 

  29. Martins, C., de Resende, M., da Silva, D., Magalhães, T., Modolo, L., Pilli, R., and de Fátima, A., J. Appl. Microbiol., 2009, vol. 107, pp. 1279–1286. https://doi.org/10.1111/j.1365-2672.2009.04307.x

    Article  CAS  PubMed  Google Scholar 

  30. Karthikeyan, M.S., Prasad, D.J., Poojary, B., Bhat, K.S., Holla, B.S., and Kumari, N.S., Bioorg. Med. Chem., 2006, vol. 14, pp. 7482–7489. https://doi.org/10.1016/j.bmc.2006.07.015

    Article  CAS  PubMed  Google Scholar 

  31. Echevarria, A., Nascimento, M.D.G., Gerônimo, V., Miller, J., and Giesbrecht, A., J. Braz. Chem. Soc., 1999, vol. 10, pp. 60–64. https://doi.org/10.1590/S0103-50531999000100010

    Article  CAS  Google Scholar 

  32. Pandeya, S., Sriram, D., Nath, G., and De Clercq, E., Il Farmaco, 1999, vol. 54, pp. 624–628. https://doi.org/10.1016/S0014-827X(99)00075-0

    Article  CAS  PubMed  Google Scholar 

  33. Pandeya, S., Sriram, D., Nath, G., and DeClercq, E., Eur. J. Pharm. Sci., 1999, vol. 9, pp. 25–31. https://doi.org/10.1016/S0928-0987(99)00038-X

    Article  CAS  PubMed  Google Scholar 

  34. Panneerselvam, P., Nair, R.R., Vijayalakshmi, G., Subramanian, E.H, and Sridhar, S.K., Eur. J. Med. Chem., 2005, vol. 40, pp. 225–229. https://doi.org/10.1016/j.ejmech.2004.09.003

    Article  CAS  PubMed  Google Scholar 

  35. Domb, A.J., Linden, G., Polacheck, I., and Benita, S., Polym. Chem., 1996, vol. 34, pp. 1229–1236. https://doi.org/10.1002/(SICI)1099-0518(199605)34:7%3C1229::AID-POLA9%3E3.0.CO;2-Y

    Article  CAS  Google Scholar 

  36. Qin, W., Long, S., Panunzio, M., and Biondi, S., Molecules, 2013, vol. 18, pp. 12264–12289. https://doi.org/10.3390/molecules181012264

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Largeron, M. and Fleury, M.B., Science, 2013, vol. 339, pp. 43–44. https://doi.org/10.1126/science.1232220

    Article  PubMed  Google Scholar 

  38. Liu, X., Ling, Z., Li, L., and Ruan, B., Int. J. Inf. Dis., 2011, vol. 15, pp. e298–e304. https://doi.org/10.1016/j.ijid.2011.01.005

  39. Pawar, O., Patekar, A., Khan, A., Kathawate, L., Haram, S., Markad, G., and Salunke-Gawali, S., J. Mol. Struct., 2014, vol. 1059, pp. 68–74. https://doi.org/10.1016/j.molstruc.2013.11.029

    Article  CAS  Google Scholar 

  40. Khan, F.A., Maalik, A., Iqbal, Z., and Malik, I., Eur. J. Pharmacol., 2013, vol. 721, pp. 391–394. https://doi.org/10.1016/j.ejphar.2013.05.003

    Article  CAS  PubMed  Google Scholar 

  41. Shanmugam, M., Narayanan, K., Mahalakshmi, M., Kabilan, S., and Chidambaranathan, V., Spectrochim. Acta A Mol. Biomol. Spectrosc., 2013, vol. 116, pp. 394–400. https://doi.org/10.1016/j.saa.2013.07.084

    Article  CAS  PubMed  Google Scholar 

  42. Sumrra, S.H. and Chohan, Z.H., J. Enzyme Inhibit. Med. Chem., 2013, vol. 28, pp. 1291–1299. https://doi.org/10.3109/14756366.2012.735666

    Article  CAS  Google Scholar 

  43. Jin, X., Wang, J., and Bai, J., Carbohydr. Res., 2009, vol. 344, pp. 825–829. https://doi.org/10.1016/j.carres.2009.01.022

    Article  CAS  PubMed  Google Scholar 

  44. Silva, S., J. Bot., 2012, vol. 2012, pp. 1–8. https://doi.org/10.1155/2012/219462

    Article  CAS  Google Scholar 

  45. Aboul-Fadl, T., Bin-Jubair, F.A., and Aboul-Wafa, O., Eur. J. Med. Chem., 2010, vol. 45, pp. 4578–4586. https://doi.org/10.1016/j.ejmech.2010.07.020

    Article  CAS  PubMed  Google Scholar 

  46. Prakash, C.R. and Raja, S., J. Saudi Chem. Soc., 2013, vol. 17, pp. 337–344. https://doi.org/10.1016/j.jscs.2011.10.022

    Article  CAS  Google Scholar 

  47. Alam, R., MSc Thesis, 2018, University of Engineering and Technology (Buet) Dhaka-1000, Bangladesh. https://lib.buet.ac.bd:8080/xmlui/handle/123456789/5178

  48. Baquero, F., J. Antimicrob. Chemother., 1997, vol. 39, pp. 1–6. https://doi.org/10.1093/ac/39.suppl_1.1

    Article  CAS  PubMed  Google Scholar 

  49. Alekshun, M.N. and Levy, S.B., Cell, 2007, vol. 128, pp. 1037–1050. https://doi.org/10.1016/j.cell.2007.03.004

    Article  CAS  PubMed  Google Scholar 

  50. Shi, L., Ge, H.M., Tan, S.H., Li, H.Q., Song, Y.C., Zhu, H.L., and Tan, R.X., Eur. J. Med. Chem., 2007, vol. 42, pp. 558–564. https://doi.org/10.1016/j.ejmech.2006.11.010

    Article  CAS  PubMed  Google Scholar 

  51. Hearn, M.J. and Cynamon, M.H., J. Antimicrob. Chemother., 2004, vol. 53, pp. 185–191. https://doi.org/10.1093/jac/dkh041

    Article  CAS  PubMed  Google Scholar 

  52. Paulus, E., Dornberger, K., Werner, W., and Fenske, D., Acta Crystallogr. Sec. C: Cryst. Struct. Commun., 1994, vol. 50, pp. 2064–2067. https://doi.org/10.1107/S0108270194003185

    Article  Google Scholar 

  53. Heinisch, L., Roemer, E., Juetten, P., Haas, W., Werner, W., and Moellmann, U., J. Antibiot., 1999, vol. 52, pp. 1029–1041. https://doi.org/10.7164/antibiotics.52.1029

    Article  CAS  Google Scholar 

  54. Baluja, S., Solank, A., and Kachhadia, N., J. Iran. Chem. Soc., 2006, vol. 3, pp. 312–317. https://link.springer.com/article/10.1007/BF03245952

    Article  CAS  Google Scholar 

  55. Chohan, Z.H., Arif, M., and Sarfraz, M., J. Appl. Organomet. Chem., 2007, vol. 21, pp. 294–302. https://doi.org/10.1002/aoc.1200

    Article  CAS  Google Scholar 

  56. Yildiz, M., Kĺraz, A., and Dülger, B., J. Serbi. Chem. Soc., 2007, vol. 72, pp. 215–224. https://doi.org/10.2298/JSC0703215Y

    Article  CAS  Google Scholar 

  57. Venugopala, K. and Jayashree, B., Indian J. Pharm. Sci., 2008, vol. 70, p. 88. https://doi.org/10.4103/0250-474X.40338

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Abdallah, S.M., Mohamed, G.G., Zayed, M., and Abou El-Ela, M.S., Mol. Biomol. Spectros., 2009, vol. 73, pp. 833–840. https://doi.org/10.1016/j.saa.2009.04.005.Epub2009Apr22

    Article  Google Scholar 

  59. Bayrak, H., Demirbas, A., Karaoglu, S.A., and Demirbas, N., Eur. J. Med. Chem., 2009, vol. 44, pp. 1057–1066. https://doi.org/10.1016/j.ejmech.2008.06.019

    Article  CAS  PubMed  Google Scholar 

  60. Theuretzbacher, U., Int. Antimicrob. Agent, 2012, vol. 39, pp. 295–299. https://doi.org/10.1016/j.ijantimicag.2011.12.006

    Article  CAS  Google Scholar 

  61. Şakıyan, İ., Özdemir, R., and Öğütcsü, H., Synthesis React. Inorg., Metal-Org., Nano-Metal Chem., 2014, vol. 44, pp. 417–423. https://doi.org/10.1080/15533174.2013.776604

    Article  CAS  Google Scholar 

  62. Wang, Z., Gao, J., Wang, J., Jin, X., Zou, M., Li, K., and Kang, P., Spectrochim. Acta A: Mol. Biomol. Spectros., 2011, vol. 83, pp. 511–517. https://doi.org/10.1016/j.saa.2011.08.076

    Article  CAS  Google Scholar 

  63. Makawana, J.A., Sun, J., and Zhu, H.L., Bioorg. Med. Chem. Lett., 2013, vol. 23, pp. 6264–6268. https://doi.org/10.1016/j.bmcl.2013.09.086

    Article  CAS  PubMed  Google Scholar 

  64. Adly, O.M., Spectrochim. Acta A: Mol. Biomol. Spectrosc., 2012, vol. 95, pp. 483–490. https://doi.org/10.1016/j.saa.2012.04.030

    Article  CAS  PubMed  Google Scholar 

  65. Chohan, Z.H., Shad, H.A., and Supuran, C.T., J. Enzyme Inhib. Med. Chem., 2012, vol. 27, pp. 58–68. https://doi.org/10.3109/14756366.2011.574623

    Article  CAS  PubMed  Google Scholar 

  66. Bhat, M.A., Al-Omar, M.A., and Siddiqui, N., Med. Chem. Res., 2013, vol. 22, pp. 4455–4458. https://link.springer.com/article/10.1007/s00044-012-0452-9

    Article  CAS  Google Scholar 

  67. De Clercq, E. and Herdewijn, P., Pharm. Sci. Encyclo.: Drug Dis., Dev., Manufact., 2010, pp. 1–56. https://doi.org/10.1002/9780470571224.pse026

  68. Wang, P.H., Keck, J.G., Lien, E.J., and Lai, M.M., J. Med. Chem., 1990, vol. 33, pp. 608–614. https://doi.org/10.1021/jm00164a023

    Article  CAS  PubMed  Google Scholar 

  69. Sriram, D., Yogeeswari, P., Myneedu, N. S., and Saraswat, V., Bioorg. Med. Chem. Lett., 2006, vol. 16, pp. 2127–2129. https://doi.org/10.1016/j.bmcl.2006.01.050

    Article  CAS  PubMed  Google Scholar 

  70. Marschall, M., Niemann, I., Kosulin, K., Bootz, A., Wagner, S., Dobner, T., and Vitt, D., Ant. Res., 2013, vol. 100, pp. 640–648. https://doi.org/10.1016/j.antiviral.2013.10.003

    Article  CAS  Google Scholar 

  71. Abbas, S.Y., Farag, A.A., Ammar, Y.A., Atrees, A.A., Mohamed, A.F., and El-Henawy, A.A., Monatsh. Für Chem., 2013, vol. 144, pp. 1725–1733. https://doi.org/10.1007/s00706-013-1034-3

    Article  CAS  Google Scholar 

  72. Murtaza, G., Mumtaz, A., Khan, F.A., Ahmad, S., Azhar, S., Najam-Ul-Haq, M., and Alam, F., Acta Pol. Pharm., 2014, vol. 71, pp. 531–535. https://www.ptfarm.pl/pub/File/Acta_Poloniae/1998/acta4-2014.pdf#page=11

    PubMed  Google Scholar 

  73. De Clercq, E., Antiviral research at the Rega Institute (KU Leuven), now 50 years old. In: SAGE Publications Sage 2014, UK: London, England. https://doi.org/10.1177/095632020401500501

  74. Kumar, K.S., Ganguly, S., Veerasamy, R., and De Clercq, E., Eur. J. Med. Chem., 2010, vol. 45, pp. 5474–5479. https://doi.org/10.1016/j.ejmech.2010.07.058

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  75. Ali, I., Haque, A., Saleem, K., and Hsieh, M.F., Bioorg. Med. Chem., 2013, vol. 21, pp. 3808–3820. https://doi.org/10.1016/j.bmc.2013.04.018

    Article  CAS  PubMed  Google Scholar 

  76. Sondhi, S.M., Arya, S., Rani, R., Kumar, N., and Roy, P., Med. Chem. Res., 2012, vol. 21, pp. 3620–3628. https://doi.org/10.1007/s00044-011-9899-3

    Article  CAS  Google Scholar 

  77. Tabassum, S., Amir, S., Arjmand, F., Pettinari, C., Marchetti, F., Masciocchi, N., and Pettinari, R., Eur. J. Med. Chem., 2013, vol. 60, pp. 216–232. https://doi.org/10.1016/j.ejmech.2012.08.019

    Article  CAS  PubMed  Google Scholar 

  78. Sathiyaraj, S., Sampath, K., Butcher, R.J., Pallepogu, R., and Jayabalakrishnan, C., Eur. J. Med. Chem., 2013, vol. 64, pp. 81–89. https://doi.org/10.1016/j.ejmech.2013.03.047

    Article  CAS  PubMed  Google Scholar 

  79. Demirbas, N., Karaoglu, S.A., Demirbas, A., and Sancak, K., Eur. J. Med. Chem., 2004, vol. 39, pp. 793–804. https://doi.org/10.1016/j.ejmech.2004.06.007

    Article  CAS  PubMed  Google Scholar 

  80. Nic, M., Jirat, J., and Kosata, B., Chem. Int., 2006, vol. 28, p. 28. https://old2015.iupac.org/publications/ci/2006/2806/2806-pp28-29.pdf

    Google Scholar 

  81. Terzioglu, N. and Gürsoy, A., Eur. J. Med. Chem., 2003, vol. 38, pp. 781–786. https://doi.org/10.1016/S0223-5234(03)00138-7

    Article  CAS  PubMed  Google Scholar 

  82. Kamel, M.M., Ali, H.I., Anwar, M.M., Mohamed, N.A., and Soliman, A.M., Eur. J. Med. Chem., 2010, vol. 45, pp. 572–580. https://doi.org/10.1016/j.ejmech.2009.10.044

    Article  CAS  PubMed  Google Scholar 

  83. Gürsoy, E. and Güzeldemirci, N.U., Eur. J. Med. Chem., 2007, vol. 42, pp. 320–326. https://doi.org/10.1016/j.ejmech.2006.10.012

    Article  CAS  PubMed  Google Scholar 

  84. Shabani, F., Saghatforoush, L.A., and Ghammamy, S., Bul. Chem. Soc. Ethiop., 2010, vol. 24, pp. 193–199. https://doi.org/10.4314/bcse.v24i2.54741

    Article  CAS  Google Scholar 

  85. Joginder, K., Amit, R., and Vinit, R., Org. Med. Chem. Int. J., 2017, vol. 1, p. 15. https://doi.org/10.19080/OMCIJ.2017.01.555564

    Article  Google Scholar 

  86. Hu, G., Wang, G., Duan, N., Wen, X., Cao, T., Xie, S., and Huang, W., Acta Pharm. Sin. B, 2012, vol. 2, pp. 312–317. https://doi.org/10.1016/j.apsb.2011.11.003

    Article  CAS  Google Scholar 

  87. Creaven, B.S., Duff,B., Egan, D.A., Kavanagh, K., Rosair, G., Thangella, V.R., and Walsh, M., J. Inorg. Chim. Acta, 2010, vol. 363, pp. S4048–S4058. https://doi.org/10.1016/j.ica.2010.08.009

  88. Sunil, D., Isloor, A.M., Shetty, P., Nayak, P.G., and Pai, K., Arabian J. Chem., 2013, vol. 6, pp. 25–33. https://doi.org/10.1016/j.arabjc.2010.12.016

    Article  CAS  Google Scholar 

  89. Kajal, A., Bala, S., Kamboj, S., Sharma, N., and Saini, V., J. Catal., 2013, vol. 2013, Article ID: 893512. https://doi.org/10.1155/2013/893512

  90. Li, G., Zhang, H., Wang, R., He, Y., and Xiong, Y., Chin. Sci. Bull., 2013, vol. 58, pp. 2956–2963. https://doi.org/10.1007/s11434-013-5787-1

    Article  CAS  Google Scholar 

  91. Sharma, U.K., Sood, S., Sharma, N., Rahi, P., Kumar, R., Sinha, A.K., and Gulati, A., Med. Chem. Res., 2013, vol. 22, pp. 5129–5140. https://doi.org/10.1007/s00044-013-0484-9

    Article  CAS  Google Scholar 

  92. Ramírez-Jiménez, A., Luna-García, R., Cortés-Lozada, A., Hernández, S., Ramírez-Apan, T., Nieto-Camacho, A., and Gómez, E., J. Organomet. Chem., 2013, vol. 738, pp. 10–19. https://doi.org/10.1016/j.jorganchem.2013.03.038

    Article  CAS  Google Scholar 

  93. Kumar, D. and Rawat, D.S., Bioorg. Med. Chem. Lett., 2013, vol. 23, pp. 641–645. https://doi.org/10.1016/j.bmcl.2012.12.001

    Article  CAS  PubMed  Google Scholar 

  94. Zhang, Y., Fang, Y., Liang, H., Wang, H., Hu, K., Liu, X., and Peng, Y., Bioorg. Med. Chem. Lett., 2013, vol. 23, pp. 107–111. https://doi.org/10.1016/j.bmcl.2012.11.006

    Article  CAS  PubMed  Google Scholar 

  95. Valentina, P., Ilango, K., Deepthi, M., Harusha, P., Pavani, G., Sindhura, K.L., and Keerthanan, C.G., J. Pharm. Sci. Res., 2009, vol. 1, p. 74. https://citeseerx.ist.psu.edu/document?repid=rep1&type=pdf&doi=13b0908e996b89de25ab617abb72cc8493aadbcd

    CAS  Google Scholar 

  96. Bala, S., Uppal, G., Kamboj, S., Saini, V., and Prasad, D., Med.l Chem. Res., 2013, vol. 22, pp. 2755–2767. https://link.springer.com/article/10.1007/s00044-012-0270-0

    Article  CAS  Google Scholar 

  97. Wu, H., Jia, F., Kou, F., Liu, B., Yuan, J., and Bai, Y., Transit. Met. Chem., 2011, vol. 36, pp. 847–853. https://doi.org/10.1080/00958972.2011.624180

    Article  CAS  Google Scholar 

  98. Smith, C.J., Zhang, Y., Koboldt, C.M., Muhammad, J., Zweifel, B.S., Shaffer, A., and Isakson, P.C., Proc. Nati. Acad. Sci., 1998, vol. 95, pp. 13313–13318. https://doi.org/10.1073/pnas.95.22.13313

    Article  CAS  Google Scholar 

  99. Warner, T.D., Giuliano, F., Vojnovic, I., Bukasa, A., Mitchell, J.A., and Vane, J.R., Proc. Nati. Acad. Sci., 1999, vol. 96, pp. 7563–7568. https://doi.org/10.1073/pnas.96.13.7563

    Article  CAS  Google Scholar 

  100. Bhandari, S.V., Bothara, K.G., Raut, M.K., Patil, A.A., Sarkate, A.P., and Mokale, V.J., Bioorg. Med. Chem., 2008, vol. 16, pp. 1822–1831. https://doi.org/10.1016/j.bmc.2007.11.014

    Article  CAS  PubMed  Google Scholar 

  101. Alam, M.S., Choi, J.H., and Lee, D.U., Bioorg. Med. Chem., 2012, vol. 20, pp. 4103–4108. https://doi.org/10.1016/j.bmc.2012.04.058

    Article  CAS  PubMed  Google Scholar 

  102. Iqbal, M.S., Khurshid, S.J., and Muhammad, B., Med. Chem. Res., 2013, vol. 22, pp. 861–868. https://doi.org/10.1007/s00044-012-0068-0

    Article  CAS  Google Scholar 

  103. Bawa, S. and Kumar, S., Int. J. Cent. Bank, 2009, pp. 142–145. https://nopr.niscpr.res.in/bitstream/123456789/2938/1/IJCB%2048B%281%29%20142-145.pdf

  104. Lima, P.C., Lima, L.M., da Silva, K.C.M., Léda, P.H.O., de Miranda, A.L.P., Fraga, C.A., and Barreiro, E.J., Eur. J. Med. Chem., 2000, vol. 35, pp. 187–203. https://doi.org/10.1016/S0223-5234(00)00120-3

    Article  CAS  PubMed  Google Scholar 

  105. Panneerselvam, P., Priya, M.G., Kumar, N.R., and Saravanan, G., Indian J. Pharm. Sci., 2009, vol. 71, p. 428. https://doi.org/10.4103/0250-474X.57292

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  106. Kalluraya, B., Aamir, S., and Shabaraya, A., Eur. J. Med. Chem., 2012, vol. 54, pp. 597–604. https://doi.org/10.1016/j.ejmech.2012.06.011

    Article  CAS  PubMed  Google Scholar 

  107. Zheng, Y., Ma, K., Li, H., Li, J., He, J., Sun, X., and Ma, J., Catal. Lett., 2009, vol. 128, pp. 465–474. https://doi.org/10.1007/s10562-008-9774-0

    Article  CAS  Google Scholar 

  108. Rabjohn, N., Organic Syntheses: Being a Revised Edition of Annual Volumes 30–39, John Wiley and Sons. 1963. https://doi.org/10.1126/science.142.3589.221.b

  109. Westheimer, F. and Taguchi, K., J. Org. Chem., 1971, vol. 36, pp. 1570–1572. https://doi.org/10.1021/jo00810a033s

    Article  CAS  Google Scholar 

  110. Love, B.E. and Ren, J., J. Org. Chem., 1993, vol. 58, pp. 5556–5557. https://doi.org/10.1021/jo00072a051

    Article  CAS  Google Scholar 

  111. Look, G.C., Murphy, M.M., Campbell, D.A., and Gallop, M.A., Tetrahedr. Lett., 1995, vol. 36, pp. 2937–2940. https://doi.org/10.1016/0040-4039(95)00442-F

    Article  CAS  Google Scholar 

  112. Chakraborti, A.K., Bhagat, S., and Rudrawar, S., Tetrahedr. Lett., 2004, vol. 45, pp. 7641–7644. https://doi.org/10.1016/j.tetlet.2004.08.097

    Article  CAS  Google Scholar 

  113. Kulkarni, A., Patil, S.A., and Badami, P.S., Eur. J. Med. Chem., 2009, vol. 44, pp. 2904–2912. https://doi.org/10.1016/j.ejmech.2008.12.012

    Article  CAS  PubMed  Google Scholar 

  114. Naeimi, H., Salimi, F., and Rabiei, K., J. Mol. Catal. A: Chem., 2006, vol. 260, pp. 100–104. https://doi.org/10.1016/j.molcata.2006.06.055

    Article  CAS  Google Scholar 

  115. Dalpozzo, R., De Nino, A., Nardi, M., Russo, B., and Procopio, A., Synthesis, 2006, vol. 2006, pp. 1127–1132. https://doi.org/10.1055/s-2006-926378

    Article  CAS  Google Scholar 

  116. Baricordi, N., Benetti, S., Biondini, G., De Risi, C., and Pollini, G.P., Tetrahedr. Lett., 2004, vol. 45, pp. 1373–1375. https://doi.org/10.1016/j.tetlet.2003.12.071

    Article  CAS  Google Scholar 

  117. Samec, J.S. and Bäckvall, J.E., Chem.–A Eur. J., 2002, vol. 8, pp. 2955–2961. https://doi.org/10.1002/1521-3765(20020703)8:13%3C2955::AID-CHEM2955%3E3.0.CO;2-Q

    Article  CAS  Google Scholar 

  118. Gheorghe RomanI, M.A., Bull. Chem. Technol. Maced., 2011, vol. 20, pp. 131–136. https://rb.gy/uzsxd8

    Google Scholar 

  119. Liu, G., Cogan, D.A., Owens, T.D., Tang, T.P., and Ellman, J.A., J. Org. Chem., 1999, vol. 64, pp. 1278–1284. https://doi.org/10.1021/jo982059i

    Article  CAS  Google Scholar 

  120. Armstrong, J.D. III, Wolfe, C.N., Keller, J.L., Lynch, J., Bhupathy, M., Volante, R., and De Vita, R.J., Tetrahedr. Lett., 1997, vol. 38, pp. 1531–1532. https://doi.org/10.1016/S0040-4039(97)00149-4

    Article  CAS  Google Scholar 

  121. Branchaud, B.P., J. Org. Chem., 1983, vol. 48, pp. 3531–3538. https://pubs.acs.org/doi/abs/10.1021/jo00168a031

    Article  CAS  Google Scholar 

  122. White, W.A. and Weingarten, H., J. Org. Chem., 1967, vol. 32, pp. 213–214. https://doi.org/10.1021/jo01277a052

    Article  CAS  Google Scholar 

  123. Billman, J.H. and Tai, K.M., J. Org. Chem., 1958, vol. 23, pp. 535–539. https://pubs.acs.org/doi/pdf/10.1021/jo01098a009

    Article  CAS  Google Scholar 

  124. Gedye, R., Smith, F., Westaway, K., Ali, H., and Baldisera, L., Tetrahedr. Lett., 1986, vol. 27, pp. 279–282. https://doi.org/10.1016/S0040-4039(00)83996-9

    Article  CAS  Google Scholar 

  125. Giguere, R.J., Bray, T.L., Duncan, S.M., and Majetich, G., Tetrahedr. Lett., 1986, vol. 27, pp. 4945–4948. https://doi.org/10.1016/S0040-4039(00)85103-5

    Article  CAS  Google Scholar 

  126. Varma, R.S., Dahiya, R., and Kumar, S., Tetrahedr. Lett., 1997, vol. 38, pp. 2039–2042. https://doi.org/10.1016/S0040-4039(97)00261-X

    Article  CAS  Google Scholar 

  127. Schmeyers, J., Toda, F., Boy, J., and Kaupp, G., J. Chem. Soc., Perkin Transactions, 1998, vol. 2, pp. 989–994. https://doi.org/10.1039/A704633B

    Article  Google Scholar 

  128. Vass, A., Dudás, J., and Varma, R.S., Tetrahedr. Lett., 1999, vol. 40, pp. 4951–4954. https://doi.org/10.1016/S0040-4039(99)00867-9

    Article  CAS  Google Scholar 

  129. Tanaka, K. and Shiraishi, R., Green Chem., 2000, vol. 2, pp. 272–273. https://doi.org/10.1039/B006424F

    Article  CAS  Google Scholar 

  130. Andrade, C.K.Z., Takada, S.C.S., Alves, L.M., Rodrigues, J.P., Suarez, P.A.Z., Brandao, R.F., and Soares, V.C.D., Synlett, 2004, vol. 2004, pp. 2135–2138. https://doi.org/10.1055/s-2004-831328

    Article  CAS  Google Scholar 

  131. Vázquez, M.Á., Landa, M., Reyes, L., Miranda, R., Tamariz, J., and Delgado, F., Synth. Commun., 2004, vol. 34, pp. 2705–2718. https://doi.org/10.1081/SCC-200026190

    Article  CAS  Google Scholar 

  132. Gopalakrishnan, M., Sureshkumar, P., Kanagarajan, V., Thanusu, J., and Govindaraju, R., J. Chem. Res., 2005, vol. 2005, pp. 299–303. https://doi.org/10.3184/0308234054323977

    Article  Google Scholar 

  133. Gopalakrishnan, M., Sureshkumar, P., Kanagarajan, V., and Thanusu, J. Res. Chem. Interm., 2007, vol. 33, pp. 541–548. https://doi.org/10.1163/156856707782565822

    Article  CAS  Google Scholar 

  134. Guzen, K.P., Guarezemini, A.S., Orfao, A.T., Cella, R., Pereira, C.M., and Stefani, H.A., Tetrahedr. Lett., 2007, vol. 48, pp. 1845–1848. https://doi.org/10.1016/j.tetlet.2007.01.014

    Article  CAS  Google Scholar 

  135. Rao, G.K., Kaur, R., and Pai, P., J. Chem. Pharm. Res., 2010, vol. 2, pp. 489–496. https://shorturl.at/ovKNY

    CAS  Google Scholar 

  136. Chohan, Z.H. and Mushtaq, S., Pak. J. Pharm. Sci., 2000, vol. 13, pp. 21–27. https://europepmc.org/article/med/16414835

    CAS  PubMed  Google Scholar 

  137. Thangadurai, T.D. and Ihm, S.K., J. Ind. Eng. Chem., 2003, vol. 9, pp. 563–568. https://www.cheric.org/research/tech/periodicals/view.php?seq=426724

    CAS  Google Scholar 

  138. Thangadurai, T.D. and Ihm, S.K., Synth. React. Inorg., Metal-Org., Nano-Metal Chem., 2005, vol. 35, pp. 499–507. https://sci-hub.hkvisa.net/10.1081/SIM-200067062

    Article  CAS  Google Scholar 

  139. Mohamed, G.G., Omar, M.M., and Hindy, A.M., Turk. J. Chem., 2006, vol. 30, pp. 361–382. https://journals.tubitak.gov.tr/chem/vol30/iss3/11/

    CAS  Google Scholar 

  140. Siddiqi, K., Kureshy, R., Khan, N., Tabassum, S., and Zaidi, S., Inorg. Chim. Acta, 1988, vol. 151, pp. 95–100. https://doi.org/10.1016/S0020-1693(00)91888-7

    Article  CAS  Google Scholar 

  141. Laidler, D.A. and Milner, D.J., J. Organomet. Chem., 1984, vol. 270, pp. 121–129. https://doi.org/10.1016/0022-328X(84)80341-1s

    Article  CAS  Google Scholar 

  142. Kozlow, N.S., Korotyshova, G.P., Rozhkova, N.G., and Andreeva, E.I., Chem. Abstr., 1987, vol. 106, p. 155955.

  143. Zhu, L.,Chen, N., Li, H., Song, F., and Zhu, X., Chem. Abst., 2004, vol. 141, p. 374026.

    Google Scholar 

  144. Gwaram, N.S., Ali, H.M., Abdulla, M.A., Buckle, M.J., Sukumaran, S.D., Chung, L.Y., and Hadi, A.H.A., Molecules, 2012, vol. 17, pp. 2408–2427. https://doi.org/10.3390/molecules17032408

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  145. Gwaram, N.S., Ali, H.M., Saharin, S.M., Abdulla, M.A., Hassandarvish, P., Lin, T.K., and Ooi, C.L., J. Appl. Pharm. Sci., 2012, vol. 2, p. 27. https://doi.org/10.7324/JAPS.2012.21206

    Article  Google Scholar 

  146. Kostova, I. and Saso, L., Curr. Med. Chem., 2013, vol. 20, pp. 4609–4632. https://www.ingentaconnect.com/content/ben/cmc/2013/00000020/00000036/art00010

    Article  CAS  PubMed  Google Scholar 

  147. Alizadeh, N., Ershad, S., Naeimi, H., Sharghi, H., and Shamsipur, M., Pol. J. Chem., 1999, vol. 73, pp. 915–925. https://www.infona.pl/resource/bwmeta1.element.baztech-article-BUJ2-0003-0003

    CAS  Google Scholar 

  148. Fernández-G, J., del Rio-Portilla, F., Quiroz-Garcıa, B., Toscano, R., and Salcedo, R., J. Mol. Struct., 2011, vol. 561, pp. 197–207. https://doi.org/10.1016/S0022-2860(00)00915-7

    Article  Google Scholar 

  149. Ando, R., Ono, H., Yagyu, T., and Maeda, M., Inorg. Chim. Acta, 2004, vol. 357, pp. 817–823. https://doi.org/10.1016/j.ica.2003.07.005

    Article  CAS  Google Scholar 

  150. Sanz, D., Perona, A., Claramunt, R. M., and Elguero, J., Tetrahedron, 2005, vol. 61, pp. 145–154. https://doi.org/10.1016/j.tet.2004.10.036

    Article  CAS  Google Scholar 

  151. Zhu, J., Chen, L., Wu, H., and Yang, J., Chin. J. Chem., 2009, vol. 27, pp. 1868–1870. https://doi.org/10.1002/cjoc.200990313

    Article  CAS  Google Scholar 

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Dhedan, R.M., Alsahib, S.A. & Ali, R.A. A Brief Review on Schiff Base, Synthesis, and Their Antimicrobial Activities. Russ J Bioorg Chem 49 (Suppl 1), S31–S52 (2023). https://doi.org/10.1134/S1068162023080046

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