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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
 
Creator RELE, DN
BASKARAN, S
KORDE, SS
VORA, JD
TRIVEDI, GK
 
Subject ketones
 
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.
 
Publisher COUNCIL SCIENTIFIC INDUSTRIAL RESEARCH
 
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
 
Type Article
 
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
 
Language en