2006
DOI: 10.1016/j.bmcl.2006.09.019
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Synthesis and anti-microbial activity of pyrazolylbisindoles—Promising anti-fungal compounds

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Cited by 155 publications
(70 citation statements)
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“…More recently, we found that aldehydes reacted with malononitrile efficiently in the absence of catalyst and solvent under microwave irradiation and thermal heating conditions (13). 4,4?-(Arylmethylene)bis(1H-pyrazol)-5-ols are applied as fungicides (14), pesticides (15), dyestuffs (16), and as the chelating and extracting reagents for different metal ions (17). The conventional chemical approach to 4,4?-(arylmethylene)bis(3-methyl-1-phenyl-1H-pyrazo l-5-ols) involves the successive Knoevenagel synthesis of the corresponding arylidinepyrazolones and its base-promoted Michael reaction and also one-pot tandem KnoevenagelÁMichael reaction of arylaldehydes with two equivalents of 3-methyl-1-phenyl-1 *Corresponding author.…”
Section: Introductionmentioning
confidence: 99%
“…More recently, we found that aldehydes reacted with malononitrile efficiently in the absence of catalyst and solvent under microwave irradiation and thermal heating conditions (13). 4,4?-(Arylmethylene)bis(1H-pyrazol)-5-ols are applied as fungicides (14), pesticides (15), dyestuffs (16), and as the chelating and extracting reagents for different metal ions (17). The conventional chemical approach to 4,4?-(arylmethylene)bis(3-methyl-1-phenyl-1H-pyrazo l-5-ols) involves the successive Knoevenagel synthesis of the corresponding arylidinepyrazolones and its base-promoted Michael reaction and also one-pot tandem KnoevenagelÁMichael reaction of arylaldehydes with two equivalents of 3-methyl-1-phenyl-1 *Corresponding author.…”
Section: Introductionmentioning
confidence: 99%
“…16 Moreover, the corresponding 4,4'-(arylmethylene)bis(1H-pyrazol-5-ols) are used as insecticides, 17 pesticides, 18 dyestuffs, 19 and the chelating and extracting reagents for different metal ions. 20 One-pot tandem Knoevenagel-type condensation/Michael reaction between aromatic aldehydes with 2 equivalents of 3-methyl-l-phenyl-5-pyrazolone is one of the most pivotal preparation methods of 4,4'-(arylmethylene)bis(3-methyl-1-phenyl-1H-pyrazol-5-ols).…”
Section: −9mentioning
confidence: 99%
“…3 Bis(indolyl)methanes are known to promote beneficial estrogen metabolism and induce apoptosis in human cancer cell. 4a,b Other beneficial activities such as dietary supplements, 5 topoisomerase IIa inhibitors, 6 antibacterials, 7 antibiotics, 8 antifungal, 9 anti-inflammatory, 10 antimicrobialactivities, 11 agrochemicals, 12 and in material sciences as calorimetric sensors, particularly for various metals and fluorides. 13a, b Due to their broad range of biological applications, there is a great deal of interest in the synthesis of bis(indolyl)methane derivatives.…”
Section: Introductionmentioning
confidence: 99%