Synthesis, double Michael-reaction and antimicrobial activity of cross-conjugated enyone
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Title |
Synthesis, double Michael-reaction and antimicrobial activity of cross-conjugated enyone
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Creator |
RELE, DN
BASKARAN, S KORDE, SS VORA, JD TRIVEDI, GK |
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Subject |
ketones
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Description |
Synthesis of the enyones 6(a-c) has been carried out by catalyzing the reactions with CeCl3. Phase transfer catalyzed double Michael addition reactions of the enyone 6a have also been investigated. The bisannulation could be enforced through the agency of the Lindlar's catalyst. The syntheses of a substituted cyclohexenone 11 and a spiro trione 13 are also described. In addition, antimicrobial activity of all the enyones 6 and the bisbenzalacetone 14 have been reported.
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Publisher |
COUNCIL SCIENTIFIC INDUSTRIAL RESEARCH
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Date |
2011-07-21T03:20:32Z
2011-12-26T12:51:51Z 2011-12-27T05:38:31Z 2011-07-21T03:20:32Z 2011-12-26T12:51:51Z 2011-12-27T05:38:31Z 1996 |
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Type |
Article
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Identifier |
INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 35(5), 431-436
0376-4699 http://dspace.library.iitb.ac.in/xmlui/handle/10054/5760 http://hdl.handle.net/10054/5760 |
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Language |
en
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