Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/61921
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dc.contributor.authorKotha, Sambasivarao-
dc.contributor.authorAgrawal, Arpit-
dc.date.accessioned2023-05-18T05:09:52Z-
dc.date.available2023-05-18T05:09:52Z-
dc.date.issued2023-05-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/61921-
dc.description527-531en_US
dc.description.abstractA short synthetic sequence to a linear triquinane is reported involving [3+2] cycloaddition, oxidative cleavage of double bond using ruthenium catalyst followed by decarboxylation. By this methodology, norbornene double bond can be easily cleaved to obtain the linear triquinane unit. This methodology is useful for the synthesis of natural and non-natural products having fused cyclopentane ring systems.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR,Indiaen_US
dc.sourceIJC Vol.62(05) [May 2023]en_US
dc.subjectTriquinaneen_US
dc.subjectCycloadditionen_US
dc.subjectDecarboxylationen_US
dc.subjectOxidative Cleavageen_US
dc.subjectCyclopentaneen_US
dc.titleSynthesis of linear cis-anti-cis triquinane derivative via a [3+2] cycloaddition and Krapcho decarboxylation as key stepsen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v62i5.1433en_US
Appears in Collections:IJC Vol.62(05) [May 2023]

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