2014
DOI: 10.1007/s00044-014-1180-0
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Synthesis and antimicrobial activity of pyrazolyl benzoxazoles, benzothiazoles and benzimidazoles

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Cited by 13 publications
(3 citation statements)
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“…Reddy et al, reported the synthesis of a new class of pyrazolyl–benzimidazoles 23a – 23c possessing an amide group by reaction between pyrazolones 21a – 21c with 1 H -benzo[d]imidazol-2-amine 9 , and the oxidation of the intermediate compounds 22a – 22c with chloranil ( Scheme 7 ) [ 61 ]. It was found that the presence of electron-withdrawing substituent “Cl” on the aromatic ring increases the antimicrobial activity, compound 23c being a potent antifungal agent against A. niger considering ketoconazole as standard.…”
Section: Synthesis Antimicrobial Activities Of Benzimidazole–pyrazole Compounds Benzimidazole–pyrazole Compounds As Potent Dna Gyrase Andmentioning
confidence: 99%
“…Reddy et al, reported the synthesis of a new class of pyrazolyl–benzimidazoles 23a – 23c possessing an amide group by reaction between pyrazolones 21a – 21c with 1 H -benzo[d]imidazol-2-amine 9 , and the oxidation of the intermediate compounds 22a – 22c with chloranil ( Scheme 7 ) [ 61 ]. It was found that the presence of electron-withdrawing substituent “Cl” on the aromatic ring increases the antimicrobial activity, compound 23c being a potent antifungal agent against A. niger considering ketoconazole as standard.…”
Section: Synthesis Antimicrobial Activities Of Benzimidazole–pyrazole Compounds Benzimidazole–pyrazole Compounds As Potent Dna Gyrase Andmentioning
confidence: 99%
“…Several methods for synthesis of 2-aminobenzoxazoles have been reported (Scheme ). , However, most of these methods suffer from specific drawbacks. The most published protocol comprises the cyclization of 2-aminophenols using BrCN as a cyanating agent, , , but this BrCN reagent is highly toxic.…”
Section: Introductionmentioning
confidence: 99%
“… , However, most of these methods suffer from specific drawbacks. The most published protocol comprises the cyclization of 2-aminophenols using BrCN as a cyanating agent, , , but this BrCN reagent is highly toxic. The next reported approach is the direct 2-C amination of benzoxazoles, but its drawbacks include the use of transition metal catalysts, high temperatures, nitrogen atmosphere, or co-oxidants.…”
Section: Introductionmentioning
confidence: 99%