Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1798
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dc.contributor.authorBeena James-
dc.contributor.authorViji, S-
dc.contributor.authorSoumini Mathew-
dc.contributor.authorMangalam S Nair-
dc.contributor.authorDivya, L-
dc.contributor.authorAjay Kumar, R-
dc.date.accessioned2015-02-23T09:15:06Z-
dc.date.available2015-02-23T09:15:06Z-
dc.date.issued2007-
dc.identifier.citationTetrahedron Letters 48(35):6204-6208;27 Aug 2007en_US
dc.identifier.issn0040-4039-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1798-
dc.description.abstractThe synthesis of novel polycyclic amides has been achieved through the reaction of bishalomethyl pentacyclo[5.4.0.0(2.6).0(3.10).0(5.9)]undecane diones with acyclic and cyclic secondary amines in the presence of an ionic liquid. Three of the compounds prepared have been found to possess antituberculosis activity.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectNeuroprotective activityen_US
dc.subjectParkinsons-diseaseen_US
dc.subjectAminesen_US
dc.subjectTuberculosisen_US
dc.subjectAmantadineen_US
dc.subjectMemantineen_US
dc.titleSynthesis of novel highly functionalized biologically active polycyclic caged amidesen_US
dc.typeArticleen_US
niist.citation-
Appears in Collections:2007

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