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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2837
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-14T13:12:31Z-
dc.date.available2021-10-14T13:12:31Z-
dc.date.issued2017-02-16-
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/00397911.2016.1278232-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2837-
dc.description.abstractA simple and efficient protocol has been developed for the synthesis of 3-alkenylated indoles and bis(indol-3-yl) derivatives by sulfonic acid-functionalized ionic liquid-catalyzed reaction of indole with 1,3-diketones/3-ketoesters under solvent-free ultrasound irradiation. Good to excellent yields (68–94%) are obtained in ultrasonication. The product of reaction is dependent on the substituent at C-2 position of indole. The catalyst is reusable and recyclable up to four cycles without significant loss of its catalytic activity. Compared with conventional heating, sound wave activation has the considerable advantages such as shorter reaction time, easy work-up, higher yields, and mild conditions.en_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.subjectChemistryen_US
dc.subject3-Alkenylated indolesen_US
dc.subjectBis(indol-3-yl) derivativesen_US
dc.subjectSolvent-free conditionen_US
dc.titleSynthesis of 3-alkenylated indole and bis(indol-3-yl) derivatives catalyzed by sulfonic acid-functionalized ionic liquid under ultrasound irradiationen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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