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Synthesis of 3-alkenylated indole and bis(indol-3-yl) derivatives catalyzed by sulfonic acid-functionalized ionic liquid under ultrasound irradiation

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dc.contributor.author Kumar, Anil
dc.date.accessioned 2021-10-14T13:12:31Z
dc.date.available 2021-10-14T13:12:31Z
dc.date.issued 2017-02-16
dc.identifier.uri https://www.tandfonline.com/doi/full/10.1080/00397911.2016.1278232
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2837
dc.description.abstract A 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.iso en en_US
dc.publisher Taylor & Francis en_US
dc.subject Chemistry en_US
dc.subject 3-Alkenylated indoles en_US
dc.subject Bis(indol-3-yl) derivatives en_US
dc.subject Solvent-free condition en_US
dc.title Synthesis of 3-alkenylated indole and bis(indol-3-yl) derivatives catalyzed by sulfonic acid-functionalized ionic liquid under ultrasound irradiation en_US
dc.type Article en_US


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