Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3200
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dc.contributor.authorKHOPADE, TUSHAR M.en_US
dc.contributor.authorSONAWANE, AMOL D.en_US
dc.contributor.authorARORA, JYOTSNA S.en_US
dc.contributor.authorBHAT, RAMAKRISHNA G.en_US
dc.date.accessioned2019-07-01T05:32:46Z
dc.date.available2019-07-01T05:32:46Z
dc.date.issued2017-11en_US
dc.identifier.citationAdvanced Synthesis & Catalysis, 359(22), 3905-3910.en_US
dc.identifier.issn1615-4150en_US
dc.identifier.issn1615-4169en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3200
dc.identifier.urihttps://doi.org/10.1002/adsc.201701084en_US
dc.description.abstractAn expedient and straightforward protocol is developed for the synthesis of highly enantiopure synthesis of γ‐butyrolactones. For the first time, one pot enantioselective organocatalytic multicomponent reaction (OMCR) is explored to construct functionalized butyrolactones without the use of pre‐functionalized substrates and expensive transition metals. The protocol is proved to be reproducible on a gram scale. Density functional theory (DFT) calculations strongly support the mechanism and were in close agreement with the observed high stereoselectivity.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectDirect Organocatalyticen_US
dc.subjectMulticomponent Synthesisen_US
dc.subjectEnantiopure-Butyrolactonesen_US
dc.subjectLactonization Sequenceen_US
dc.subjectStraightforward protocolen_US
dc.subject2017en_US
dc.titleDirect Organocatalytic Multicomponent Synthesis of Enantiopure γ‐Butyrolactones via Tandem Knoevenagel‐Michael‐Lactonization Sequenceen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleAdvanced Synthesis & Catalysisen_US
dc.publication.originofpublisherForeignen_US
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