Microwave-Induced, Iodine-Alumina Catalyzed Transformations of 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one
The chalcone derivatives, 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one was transformed to corresponding flavone derivatives by iodine impregnated neutral alumina under microwave irradiation. The synthesized flavone derivatives were structurally confirmed by elemental analysis, UV, IR...
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| Format: | Article |
| Language: | English |
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Wiley
2012-01-01
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| Series: | E-Journal of Chemistry |
| Online Access: | http://dx.doi.org/10.1155/2012/354875 |
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| _version_ | 1832563393328840704 |
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| author | P. Venkatesan K. Moorthi |
| author_facet | P. Venkatesan K. Moorthi |
| author_sort | P. Venkatesan |
| collection | DOAJ |
| description | The chalcone derivatives, 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one was transformed to corresponding flavone derivatives by iodine impregnated neutral alumina under microwave irradiation. The synthesized flavone derivatives were structurally confirmed by elemental analysis, UV, IR and 1H-NMR spectral data, and the notable yield obtained was compared with previously reported method. |
| format | Article |
| id | doaj-art-f08e17fa28b141f587ff0a686212218f |
| institution | Kabale University |
| issn | 0973-4945 2090-9810 |
| language | English |
| publishDate | 2012-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | E-Journal of Chemistry |
| spelling | doaj-art-f08e17fa28b141f587ff0a686212218f2025-02-03T01:20:24ZengWileyE-Journal of Chemistry0973-49452090-98102012-01-01921017102110.1155/2012/354875Microwave-Induced, Iodine-Alumina Catalyzed Transformations of 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-oneP. Venkatesan0K. Moorthi1Dept. of chemistry, Mahendra Institute of Technology, Namakkal – 637503, IndiaDept. of chemistry, Mahendra Institute of Technology, Namakkal – 637503, IndiaThe chalcone derivatives, 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one was transformed to corresponding flavone derivatives by iodine impregnated neutral alumina under microwave irradiation. The synthesized flavone derivatives were structurally confirmed by elemental analysis, UV, IR and 1H-NMR spectral data, and the notable yield obtained was compared with previously reported method.http://dx.doi.org/10.1155/2012/354875 |
| spellingShingle | P. Venkatesan K. Moorthi Microwave-Induced, Iodine-Alumina Catalyzed Transformations of 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one E-Journal of Chemistry |
| title | Microwave-Induced, Iodine-Alumina Catalyzed Transformations of 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one |
| title_full | Microwave-Induced, Iodine-Alumina Catalyzed Transformations of 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one |
| title_fullStr | Microwave-Induced, Iodine-Alumina Catalyzed Transformations of 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one |
| title_full_unstemmed | Microwave-Induced, Iodine-Alumina Catalyzed Transformations of 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one |
| title_short | Microwave-Induced, Iodine-Alumina Catalyzed Transformations of 1-(2′-hydroxyaryl)-3-(2-chloroquinolin-3-yl)-prop-2-en-1-one |
| title_sort | microwave induced iodine alumina catalyzed transformations of 1 2 hydroxyaryl 3 2 chloroquinolin 3 yl prop 2 en 1 one |
| url | http://dx.doi.org/10.1155/2012/354875 |
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