Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/58674
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSathya, V-
dc.contributor.authorVenkatesan, N-
dc.contributor.authorHeera, T R-
dc.contributor.authorSivakumar, M N-
dc.date.accessioned2021-12-24T04:53:43Z-
dc.date.available2021-12-24T04:53:43Z-
dc.date.issued2021-09-
dc.identifier.issn0975-0991 (Online); 0971-457X (Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/58674-
dc.description649-652en_US
dc.description.abstractSynthesis of indole based novel symmetrical nitroolefinic dendritic core has been succeeded using N-arylation route followed by Henry reaction. Synthesized symmetrical 1,3,5-triindolyl benzene has been successfully synthesis of by N-arylation of indole, symmetrical 1,3,5-tri(3-formyl indolyl)benzene and 1,3,5-tris(3-((E)-2-nitrovinyl)-1H-indol-1yl)benzene followed by Hendry reaction. These nitroolefinic cores have potential application in theoretical and medicinal chemistry and also used to prepare many new organic compounds of indole derivatives.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJCT Vol.28(5) [September 2021]en_US
dc.subjectDendritic coreen_US
dc.subjectHenry reactionen_US
dc.subjectIndoleen_US
dc.subjectN-arylationen_US
dc.subjectNitroolefinen_US
dc.titleSynthesis of indole based novel symmetrical nitroolefinic dendritic core through n-arylation routeen_US
dc.typeArticleen_US
Appears in Collections:IJCT Vol.28(5) [September 2021]

Files in This Item:
File Description SizeFormat 
IJCT 28(5) 649-652.pdf553.01 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.