A Formal Synthesis of (-)-Brasilenol

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dc.contributor.advisorKaliappan, Krishnaen_US
dc.contributor.authorCHAUHAN, TIRTHen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.contributor.registration20191159en_US
dc.date.accessioned2024-05-16T04:35:53Z
dc.date.available2024-05-16T04:35:53Z
dc.date.issued2024-05en_US
dc.description.abstractOur efforts towards a chiral pool synthesis of (-)-brasilenol from (-)-β-pinene is reported here. Starting from relatively abundant (-)-β-pinene, the unnatural enantiomer (-)-brasilenol was targeted in 11 steps. Use of stereospecific ring-opening was employed to ensure conservation of stereocenter at the isopropyl group, while hydrogenative stereospecific isomerization of exocyclic enone to endocyclic enone was utilized for prevention of racemization of the methyl group.en_US
dc.description.embargoOne Yearen_US
dc.description.sponsorshipDST INSPIREen_US
dc.identifier.citation48en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8789
dc.language.isoenen_US
dc.subjectNatural Producten_US
dc.subjectFormal Synthesisen_US
dc.subjectBrasilenolen_US
dc.subjectChiral Poolen_US
dc.titleA Formal Synthesis of (-)-Brasilenolen_US
dc.title.alternativeA Formal Synthesis of (-)-Brasilenol from Chiral Poolen_US
dc.typeThesisen_US
dc.type.degreeBS-MSen_US

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