2008
DOI: 10.3998/ark.5550190.0009.e13
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A synthesis of some new 4-arylidene-5(4H)-oxazolone azo dyes and an evaluation of their solvatochromic behaviour

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Cited by 21 publications
(2 citation statements)
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“…[2][3][4] Different sources of carbonyl functional group containing compounds are used to synthesize various Erlenmeyer products. [5][6][7][8] In addition modifications other than using different carbonyl compounds such as using other reagents than acetic anhydride such as triphenylphosphine 9 are used for the Erlenmeyer reaction. Preparation of oxazolones [10][11][12] using acetic anhydride and α-(α-haloacyl)amino acids as starting materials was reported by Bergmann and Stern.…”
Section: Introductionmentioning
confidence: 99%
“…[2][3][4] Different sources of carbonyl functional group containing compounds are used to synthesize various Erlenmeyer products. [5][6][7][8] In addition modifications other than using different carbonyl compounds such as using other reagents than acetic anhydride such as triphenylphosphine 9 are used for the Erlenmeyer reaction. Preparation of oxazolones [10][11][12] using acetic anhydride and α-(α-haloacyl)amino acids as starting materials was reported by Bergmann and Stern.…”
Section: Introductionmentioning
confidence: 99%
“…The use of these dyes results from the combination of the properties of the azo group and several types of aromatic-substituted substrates that confer thermal and photochemical stability and an intense colour over the visible range [1]. Azo dyes are used in optical recording media [2], toners [3], ink-jet printing and oil-soluble light fast dyes [4]. They have been reported to show antineoplastic, antidiabetic, antiseptics, antibacterial, antitumour [5] and antitrypanosomal [6] activities.…”
Section: Introductionmentioning
confidence: 99%