Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3658
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dc.contributor.authorPatel, Kaushalendra-
dc.date.accessioned2021-06-16T04:36:59Z-
dc.date.available2021-06-16T04:36:59Z-
dc.date.issued2019-04-26-
dc.identifier.urihttp://hdl.handle.net/123456789/3658-
dc.description.abstractUnexpected reactions triggered by the dimethyloxosulfonium methylide led to the discovery of unconventional approaches for the synthesis of cyclopropafused tetralones. These highly functionalized structures were further elaborated in one step to privileged scaffold such as tetralones. As a whole, the results presented herein establish new diversity-oriented folding pathways.en_US
dc.language.isoenen_US
dc.publisherIISERMen_US
dc.titleSynthesis of Cyclopropanoids, and elaboration to Tetralonesen_US
dc.typeThesisen_US
dc.guideRamasastry, S.S.V.-
Appears in Collections:MS Dissertation by MP-2016

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