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Synthesis and Cyclization Reactions with Quinolinyl Keto Esters. II. Synthesis of Novel 3-Diazolylquinolinones and their Enzymic Activity
Ismail, M. M. and Mohamed, H. M. Synthesis and Cyclization Reactions with Quinolinyl Keto Esters. II. Synthesis of Novel 3-Diazolylquinolinones and their Enzymic Activity Chemical Papers, Vol.59, No. 2, 2005, -
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Document type:
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Článok z časopisu / Journal Article |
Collection:
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Chemical papers
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Attached Files |
Name |
Description |
MIMEType |
Size |
Downloads |
n592a127.pdf
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592a127.pdf |
application/pdf |
721.95KB |
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Author(s) |
Ismail, M. M. Mohamed, H. M.
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Title |
Synthesis and Cyclization Reactions with Quinolinyl Keto Esters. II. Synthesis of Novel 3-Diazolylquinolinones and their Enzymic Activity
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Journal name |
Chemical Papers
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Publication date |
2005
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Year available |
2005
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Volume number |
59
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Issue number |
2
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ISSN |
0366-6352
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Place of publication |
Poland
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Publisher |
Versita
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Collection year |
2005
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Language |
english
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Subject |
250000 Chemical Sciences 250300 Organic Chemistry
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Abstract/Summary |
Ethyl 4-(1-ethyl-4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl)-2,4-dioxobutyrate, ethyl 5-(1-ethyl-4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl)pyrazole-3-caboxylate and their acid hydrozide derivatives have been prepared and reacted with hydrazines, o-phenylenediamine, triethyl orthoformate, carbon disulfide, and thiosemicarbazides in order to obtain some new 3-substituted quinolin-2-ones as: pyrazolines, isoxazolines, imidazoles, pyrazolotriazines, thiadiazoles, and triangles. All the newly prepared compounds revealed the potent effect on increasing reactivity of cellobimse. The structure of the new compounds was established upon their elemental analyses, IR, 1H NMR, and mass fragmentation spectra.
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