SYNTHESIS, DOUBLE MICHAEL-REACTION AND ANTIMICROBIAL ACTIVITY OF CROSS-CONJUGATED ENYONE

Authors
RELE DN BASKARAN S KORDE SS VORA JD TRIVEDI GK
Citation
Dn. Rele et al., SYNTHESIS, DOUBLE MICHAEL-REACTION AND ANTIMICROBIAL ACTIVITY OF CROSS-CONJUGATED ENYONE, Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry, 35(5), 1996, pp. 431-436
Citations number
18
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry → ACNP
ISSN journal
03764699
Volume
35
Issue
5
Year of publication
1996
Pages
431 - 436
Database
ISI
SICI code
0376-4699(1996)35:5<431:SDMAAA>2.0.ZU;2-Q
Abstract
Synthesis of the enyones 6(a-c) has been carried out by catalyzing the reactions with CeCl3. Phase transfer catalyzed double Michael additio n reactions of the enyone 6a have also been investigated. The bisannul ation 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 eny ones 6 and the bisbenzalacetone 14 have been reported.