[1]
Dofe, V.S.; Sarkate, A.P.; Shaikh, Z.M.; Gill, C.H. Ultrasound mediated synthesis of novel 1,2,3-triazole based pyrazole and pyrimidine derivatives as antimicrobial agents. J. Het. Chem., 2017, 54(6), 3195-3201.
[2]
Dofe, V.S.; Sarkate, A.P.; Lokwani, D.K.; Kathwate, S.H.; Gill, C.H. Synthesis, antimicrobial evaluation, and molecular docking studies of novel chromone based 1,2,3-triazoles. Res. Chem. Int., 2017, 43(1), 15-28.
[3]
Buckle, D.R.; Rockell, C.J.M.; Smith, H.; Spicer, B.A. Studies on 1,2,3,-triazoles. 10. Synthesis and antiallergic properties of 9-oxo-1H,9H-benzothiopyrano[2,3-d]-1,2,3-triazoles and their S oxides. J. Med. Chem., 1984, 27(2), 223-227.
[4]
Doherty, W.; Adler, N.; Knox, A.; Nolan, D.; McGouran, J.; Nikalje, A.P.; Lokwani, D.; Sarkate, A.; Evans, P. Synthesis and evaluation of 1,2,3-triazole-containing vinyl and allyl sulfones as anti-trypanosomal agents. Eur. J. Org. Chem., 2017, 1, 175-185.
[5]
Elamari, H.; Slimi, R.; Chabot, G.G.; Quentin, L.; Scherman, D.; Girard, C. Synthesis and in vitro evaluation of potential anticancer activity of mono- and bis-1,2,3-triazole derivatives of bis-alkynes. Eur. J. Med. Chem., 2013, 60, 360-364.
[6]
Akhtar, T.; Hameed, S.; Al-Masoudi, N.A.; Khan, K.M. Synthesis and anti-HIV activity of new chiral 1,2,4-triazoles and 1,3,4-thiadiazoles. Heteroatom Chem., 2007, 18(3), 316-322.
[7]
Bao, G.W.; Shi, C.Y.; Xiao, Y.C.; Yong, Z.Y.; Hong, G.H.; Wu, Q.Y. Design synthesis and biological evaluation of 3-substituted triazole derivatives. Chin. Chem. Lett., 2011, 22(5), 519-522.
[8]
Phillips, O.A.; Udo, E.E.; Abdel-Hamid, M.; Varghese, R. Synthesis and antibacterial activity of novel 5-(4-methyl-1H-1,2,3-triazole) methyl oxazolidinones. Eur. J. Med. Chem., 2009, 44(8), 3217-3227.
[9]
Albadi, J.; Keshavarz, M.; Abedini, M.; Vafaie-nezhad, M. Copper iodide nanoparticles on poly(4-vinyl pyridine) as new and green catalyst for multicomponent click synthesis of 1,4-disubstituted-1,2,3-triazoles in water. Chin. Chem. Lett., 2012, 23(7), 797-800.
[10]
Rostovtsev, V.V.; Green, L.G.; Fokin, V.V.; Sharpless, K.B. A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective “ligation” of azides and terminal alkynes. Angew. Chem. Int. Ed., 2002, 41(14), 2596-2599.
[11]
Zhang, J.; Jin, G. G.; Xiao, S.; Wu, J.J.; Cao, S. Novel synthesis of 1,4,5-trisubstituted 1,2,3-triazoles via a one-pot threecomponent reaction of boronic acids, azide, and active methylene ketones. Tetrahedron, 2013, 69(10), 2352-2356.
[12]
Pereira, D.; Fernandes, P. Synthesis and antibacterial activity of novel 4-aryl-[1,2,3]-triazole containing macrolides. Bioorg. Med. Chem. Lett., 2011, 21(1), 510-513.
[13]
Kumar, D.; Reddy, V.B.; Varma, R.S. A facile and regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles using click chemistry. Tet. Lett., 2009, 50(18), 2065-2068.
[14]
González, J.; Pérez, V.M.; Jiménez, D.O.; Lopez-Valdez, G.; Corona, D.; Cuevas-Yañez, E. Effect of temperature on triazole and bistriazole formation through copper-catalyzed alkyne–azide cycloaddition. Tet. Lett., 2011, 52(27), 3514-3517.
[15]
Kushwaha, K.; Kaushik, N. Lata; Jain, S.C. Design and synthesis of novel 2H-chromen-2-one derivatives bearing 1,2,3-triazole moiety as lead antimicrobials. Bioorg. Med. Chem. Lett., 2014, 24(7), 1795-1801.
[16]
Kamal, A.; Hussaini, M.A.; Shaikh, F.; Poornachandra, Y.; Reddy, N.; Kumar, C.G.; Rajput, V.S.; Rani, C.; Sharma, R.; Khan, I.; Babu, N.J. Anti-tubercular agents. Part 8: Synthesis, antibacterial and antitubercular activity of 5-nitrofuran based 1,2,3-triazoles. Bioorg. Med. Chem. Lett., 2013, 23(24), 6842-6846.
[17]
Vantikommu, J.; Palle, S.; Reddy, P.S.; Ramanatham, V.; Khagga, M.; Pallapothula, V.R. Synthesis and cytotoxicity evaluation of novel 1,4-disubstituted 1,2,3-triazoles via CuI catalysed 1,3-dipolar cycloaddition. Eur. J. Med. Chem., 2010, 45(11), 5044-5050.
[18]
Xu, Z.; Bo, W.L.; Jun, R.L.; Chun, W.X.; Jian, F.L.; Liu, Y. Design, synthesis and antimicrobial activities of 1,2,3-triazole derivatives. Chin. Chem. Lett., 2012, 23(8), 933-935.
[19]
Xue, Z.C.; Wei, L.; Zhen, D.H.; Chun, X.K. Sodium hydridemediated synthesis of 1,5-diaryl-1,2,3-triazoles from anti-3-aryl-2,3-dibromopropanoic acids and organic azides. Chin. Chem. Lett., 2013, 24(8), 764-766.
[20]
Furniss, B.S.; Hannaford, A.J.; Smith, P.W.G.; Tatchell, A.R. Textbook of Practical Organic Chemistry, 5th ed; John Wiley & Sons, Inc.: New York, 1989.
[21]
Shelke, R.N.; Pansare, D.N.; Pawar, C.D.; Shinde, D.B.; Thore, S.N.; Pawar, R.P.; Bembalkar, S.R. Synthesis of novel 2hpyrano[2,3-d]thiazole-6-carbonitrile derivatives in aqueous medium. Res. Rev.: J. Chem., 2016, 5(2), 29-36.
[22]
Pawar, C.D.; Shinde, D.B. Synthesis and antimicrobial evaluation of novel substituted acetamido-4-subtituted-thiazole-5-indazole derivatives. Res. Rev.: J. Chem., 2016, 5(3), 28-33.
[23]
Pawar, C.D.; Pansare, D.N.; Shinde, D.B. Synthesis and antimicrobial evaluation of novel sulfonyl and amide coupling derivatives. EC Micro., 2017, 8(1), 14-28.
[24]
Aher, N.G.; Pore, V.S.; Mishra, N.N.; Kumar, A.; Shukla, P.K.; Sharma, A.; Bhat, M.K. Synthesis and antifungal activity of 1,2,3-triazole containing fluconazole analogues. Bioorg. Med. Chem. Lett., 2009, 19(3), 759-763.
[25]
Xian, L.W.; Wan, K.; Cheng, H.Z. Synthesis of novel sulfanilamidederived 1,2,3-triazoles and their evaluation for antibacterial and antifungal activities. Eur. J. Med. Chem., 2010, 45(10), 4631-4639.
[26]
Duraiswamy, B.; Mishra, S.K.; Subhashini, V.; Dhanraj, S.A.; Suresh, B. Studies on the antimicrobial potential of Mahonia leschenaultii Takeda root and root bark. Indian J. Pharm. Sci., 2006, 68(3), 389-391.
[27]
Saundane, A.R.; Rudresh, K.; Satyanarayan, N.D.; Hiremath, S.P. Pharmacological screening of 6H, 11H-Indolo [3, 2-c]isoquinolin-5-ones and their derivatives. Indian J. Pharm. Sci., 1998, 60(6), 379-983.
[28]
Therese, K.L.; Bhagyalaxmi, R.; Madhavan, H.N.; Deepa, P. Invitro susceptibility testing by agar dilution method to determine the minimum inhibitory concentrations of amphotericin B, fluconazole and ketoconazole against ocular fungal isolates. Int. J. Med. Microbiol., 2006, 24(4), 273-279.
43
2