Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/66992
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dc.contributor.authorKotha, Sambasivarao-
dc.contributor.authorReddy Keesari, Ramakrishna-
dc.date.accessioned2025-12-24T05:41:29Z-
dc.date.available2025-12-24T05:41:29Z-
dc.date.issued2025-12-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/66992-
dc.description1127-1132en_US
dc.description.abstractHerein, we described a simple synthetic strategy for the preparation of α-hydroxy, β-bromo-exo-dicyclopentadiene-1-one by following a three-step sequence. The synthetic strategy relies on operationally simple reactions and high yielding steps. The newly synthesized compounds have been characterized by NMR. As the disclosed compound α-hydroxy, β-bromo-exodicyclopentadiene- 1-one is highly functionalized but structurally similar to exo-dicyclopentadiene-1-one and it can be used a key building block for expanding the chemical space of cyclopentanoid derivatives.en_US
dc.language.isoenen_US
dc.publisherNIScPR - CSIRen_US
dc.sourceIJC Vol.64(12) [December 2025]en_US
dc.subjectBrominationen_US
dc.subjectCyclopentanoids,en_US
dc.subjectDicyclopentadiene-1-oneen_US
dc.subjectEpoxidationen_US
dc.subjectNorborneneen_US
dc.titleSynthesis of α-hydroxy, β-bromo-exo-dicyclopentadiene-1-one: A new building block for cyclopentanoidsen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v64i12.21377en_US
Appears in Collections:IJC Vol.64(12) [December 2025]

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