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Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/2883
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dc.contributor.authorKaur, J.-
dc.contributor.authorIslam, N.-
dc.contributor.authorKumar, A.-
dc.contributor.authorBhardwaj, V. K.-
dc.contributor.authorChimni, S. S.-
dc.date.accessioned2021-10-04T10:58:03Z-
dc.date.available2021-10-04T10:58:03Z-
dc.date.issued2021-10-04-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/2883-
dc.description.abstractA highly enantioselective Michael addition reaction of indolylnitroalkenes with 1,3-dicarbonyl compounds has been developed to obtain enantiomerically enriched 3-(2-nitro-1-(1-tosyl-1H-indol-3-yl) ethyl)pentane-2,4-dione derivatives in up to 98% ee using BnCPN as an organocatalyst. The transition state structure has been predicted using DFT calculationen_US
dc.language.isoen_USen_US
dc.subjectOrganocatalysisen_US
dc.subjectMichael addition reactionen_US
dc.subjectIndolylnitroalkenesen_US
dc.subjectEnantioselectiveen_US
dc.subjectDFTen_US
dc.titleOrganocatalytic enantioselective synthesis of C3 functionalized indole derivativesen_US
dc.typeArticleen_US
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