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A Catalyst Free Synthesis and In Vitro Antimicrobial Studies of a Series of Bis-Schiff Bases

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1TitleTitle of DocumentA Catalyst Free Synthesis and In Vitro Antimicrobial Studies of a Series of Bis-Schiff Bases
2CreatorAuthor's name, affiliation, country MOHAMMED ZAMIR AHMED, SHAIKH K A, ASGAR JAFAR KHAN FIRDOUS G. KHAN, ASRAR AHMED KHAN and SHAIKH KHALED
Organic Chemistry Research Laboratory, Yeshwant Mahavidyalaya, Nanded-431602 (MS), India
P.G Department of Chemistry, Sir Sayyad College of Arts, Commerce and Science, Aurangabad- 431001 (MS), India
Laboratory of Organic Synthesis, Milliya College, Beed- 43112 (MS), India
School of Chemical Sciences, Swami Ramanand Teerth Marathwada University, Nanded- 431606 (MS), India
School of Pharmacy, Swami Ramanand Teerth Marathwada University, Nanded- 431606 (MS), India
3SubjectDicipline(s) Chemical Science
3SubjectKeywords Hydrazones, Dibromosalicylaldehyde, Bis-Schiff bases, Antimicrobial activity
4DescriptionAbstract A series of bis-Schiff bases (3a-l) has been synthesized by condensation of substituted hydrazones (1a-l) with 3,5-dibromosalicylaldehyde (2) at room temperature within a short period of time under catalytic free conditions. The chemical structures of the synthesized compounds were confirmed on the basis of spectral analysis data. The bis-Schiff base derivatives (3a-l) were further screened for their in vitro antibacterial activity against plant, human pathogenic bacteria (Erwinia carotovora, Xanthomonas citri, Proteus vulgaris, Staphylococcus aureus) and antifungal (Alternaria and Curvularia lunata) studies. Compounds (3a-l) showed promising activities against S. aureus and Proteus vulgaris.
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  (4), (2013)
12LanuguageEnglish=en en
13RelationSupp.files
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