Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3646
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dc.contributor.authorHazra, Raju-
dc.date.accessioned2021-06-11T06:27:59Z-
dc.date.available2021-06-11T06:27:59Z-
dc.date.issued2018-11-
dc.identifier.urihttp://hdl.handle.net/123456789/3646-
dc.description.abstractWe present an organophosphine catalyzed MBH-type reaction of activated ynone and the outcome is the hydroacylation of α, ß-ynone, which leads to the formation of cyclopentadione-fused arenes and heteroarenes. In addition, we also present an organophosphine catalyzed intramolecular aldol reaction of keto-ynone, which is actually an organophosphine catalyzed δ'[C(sp3 )-H]- functionalization of α, ß-ynone, leading to the formation of 3-ethynyl-3-hydroxyindanones. Both the methodology occurs at mild conditions and is tolerant to a variety of functional groups and hence we are able to synthesize a series of compound having different type of functional groups with good to excellent yield.en_US
dc.language.isoenen_US
dc.publisherIISERMen_US
dc.subjectHydroacylationen_US
dc.subjectActivated Ynonesen_US
dc.title“Organophosphine Catalyzed Intramolecular Hydroacylation and δ' [C(Sp3 ) – H] Functionalization of Activated Ynones.”en_US
dc.typeThesisen_US
dc.guideRama Sastry, S. S. V.-
Appears in Collections:MS Dissertation by MP-2015

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