2018
DOI: 10.1007/s10593-018-2380-1
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Synthesis and fungicidal activity of monocyclic and fused 1,2,3-triazolium-5-olates

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Cited by 5 publications
(4 citation statements)
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“…In 2018, Glukhareva and colleagues synthesized a series of 1,2,3-triazolium-5-olates, and tested their anti-phytopathogenic fungal activities. Compound 26 showed the best effectiveness against 6 fungal strains ( Figure 10 ), including Phytophthora infestans ( P. infestans ), Cercospora arachidicola ( C. arachidicola ), Alternaria solani ( A. solani ), G.zeae , Sclerotinia sclerotiorum ( S. sclerotiorum ) and Rhizoctonia cerealis ( R. cerealis ), with inhibition rates of more than 80% at a concentration of 50 μg/mL [ 35 ].…”
Section: Antifungal Activities Of 123-triazolium Saltsmentioning
confidence: 99%
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“…In 2018, Glukhareva and colleagues synthesized a series of 1,2,3-triazolium-5-olates, and tested their anti-phytopathogenic fungal activities. Compound 26 showed the best effectiveness against 6 fungal strains ( Figure 10 ), including Phytophthora infestans ( P. infestans ), Cercospora arachidicola ( C. arachidicola ), Alternaria solani ( A. solani ), G.zeae , Sclerotinia sclerotiorum ( S. sclerotiorum ) and Rhizoctonia cerealis ( R. cerealis ), with inhibition rates of more than 80% at a concentration of 50 μg/mL [ 35 ].…”
Section: Antifungal Activities Of 123-triazolium Saltsmentioning
confidence: 99%
“…Studies have shown that the triazolium transformated from triazole have good bioactivities [ 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 ]. Molecules containing 1,2,3-triazolium units have been proven to exhibit a variety of biological activities, including antibacterial [ 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , 29 , 30 , 31 , 32 , 33 , 34 ], antifungal [ 5 , 6 , 7 , 8 , 9 , 35 ], anticancer [ 10 , 11 , 36 , 37 , 38 , 39 , 40 , 41 , 42 ], and antileishmanial [ 12 , 43 , 44 , 45 , 46 ] properties.…”
Section: Introductionmentioning
confidence: 99%
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“…1 Among these, mesoionic [1,2,3]triazole isoquinoliums have drawn particular attention because of their promising anticancer, antifungal, and antimicrobial activities. 2 Besides, they are also widely applied in the fields of supramolecular, organic catalysis, and ionic liquid chemistry. 3 However, to date, methods for the synthesis of mesoionic [1,2,3]triazole isoquinolium derivatives are limited.…”
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confidence: 99%