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Facile and Green Syntheses of Unsymmetrically Substituted 3-(1-Benzyl-1H-indol-3-yl)-2-(1-ethyl-1H-indole-3-carbonyl)-acrylonitrile and Study of their Antimicrobial Activities

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1TitleTitle of DocumentFacile and Green Syntheses of Unsymmetrically Substituted 3-(1-Benzyl-1H-indol-3-yl)-2-(1-ethyl-1H-indole-3-carbonyl)-acrylonitrile and Study of their Antimicrobial Activities
2CreatorAuthor's name, affiliation, country G. THIRUPATHI, M. VENKATANARAYANA, P. K. DUBEY and Y. BHARATHI KUMARI
Department of Chemistry, Jawaharlal Nehru Technological University, Hyderabad College of Engineering, Kukatpally, Hyderabad (A.P)-500085, India
3SubjectDicipline(s) Chemical Science
3SubjectKeywords Indole-3-carboxyaldehyde, 3-Cyanoacetylindole, Knoevenagel reaction, L-tryptophan, Physical grinding
4DescriptionAbstract Facile and green syntheses of unsymmetrically substituted-3-(1-benzyl-1H-indol-3-yl)-2-(1-ethyl-1H-indole-3-carbonyl)-acrylonitriles 5(a-d) is being reported. L-tryptophan has been utilized as an efficient and eco-friendly catalyst in the solvent free condition under the grind stone method at room temperature for Knoevenagel condensation of N-benzyl indole-3-carboxyaldehyde (2) with the active methylene compounds, 3-cyanoacetylindole 3(a-d) at room temperature to afford substituted-3-(1-benzyl-1H-indol-3-yl)-2-(1H-indole-3-carbonyl)-acrylonitrile 4(a-d) respectively. Subsequently these products were treated with DES and K2CO3 in the solvent free condition under the grind stone method at room temperature to afford the corresponding substituted-3-(1-benzyl-1H-indol-3-yl)-2- (1-ethyl-1H-indole-3-carbonyl)-acrylonitrile 5(a-d). The antibacterial and antifungal activities of 4(a-d) and 5(a-d) have been studied.
5PublishersOrganizing agency, location WWW Publications, India
6Contributor Sponsor(s) -
7DateDate (YYYY-MM-DD) -
8TypeStatus & genre Peer-reviewed Article
8TypeType
9FormateFile Formate PDF
10IdentifierUniform Resource Identifier Click Here
10IdentifierDigital Object Identifier
11SourceJournal/conference title; vol., no. (Year)Chemical Science Transactions, Volume  2 , Number  (1), (2013)
12LanuguageEnglish=en en
13RelationSupp.files
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Chemical Science Transactions | Chem Sci Trans | CST | Online Chemistry Journal | Open Access
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