Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/34089
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dc.contributor.authorVinayak, Botla-
dc.contributor.authorReddy, Marri Anil-
dc.contributor.authorChiranjeevi, Barreddi-
dc.contributor.authorChandrashekharam, Malapaka-
dc.contributor.authorPoornachandra, Y-
dc.contributor.authorKumar, Ganesh C-
dc.date.accessioned2016-04-12T05:26:10Z-
dc.date.available2016-04-12T05:26:10Z-
dc.date.issued2016-04-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/34089-
dc.description461-470en_US
dc.description.abstractIron-catalyzed cyclization of aminothiol with various aromatic and heteroaromatic aldehydes produces a variety of benzothiazoles in moderate to excellent yield. Compound 3o with one carbazole functional moiety bridged between two benzothiazole scaffolds is found promising and contributes to significant antimicrobial, MBC and anti-biofilm activities.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.55B(04) [April 2016]en_US
dc.subjectCyclizationen_US
dc.subjectIron(III) chlorideen_US
dc.subjectAnticanceren_US
dc.subjectBenzothiazolesen_US
dc.subjectAntimicrobial activityen_US
dc.subjectStaphylococcus aureusen_US
dc.titleIron-catalyzed cyclization of aminothiols: An easy access to benzothiazoles and evaluation of their antimicrobial and anti-biofilm activitiesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.55B(04) [April 2016]

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