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Direct Organocatalytic Multicomponent Synthesis of Enantiopure γ‐Butyrolactones via Tandem Knoevenagel‐Michael‐Lactonization Sequence

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dc.contributor.author KHOPADE, TUSHAR M. en_US
dc.contributor.author SONAWANE, AMOL D. en_US
dc.contributor.author ARORA, JYOTSNA S. en_US
dc.contributor.author BHAT, RAMAKRISHNA G. en_US
dc.date.accessioned 2019-07-01T05:32:46Z
dc.date.available 2019-07-01T05:32:46Z
dc.date.issued 2017-11 en_US
dc.identifier.citation Advanced Synthesis & Catalysis, 359(22), 3905-3910. en_US
dc.identifier.issn 1615-4150 en_US
dc.identifier.issn 1615-4169 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3200
dc.identifier.uri https://doi.org/10.1002/adsc.201701084 en_US
dc.description.abstract An 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.iso en en_US
dc.publisher Wiley en_US
dc.subject Direct Organocatalytic en_US
dc.subject Multicomponent Synthesis en_US
dc.subject Enantiopure-Butyrolactones en_US
dc.subject Lactonization Sequence en_US
dc.subject Straightforward protocol en_US
dc.subject 2017 en_US
dc.title Direct Organocatalytic Multicomponent Synthesis of Enantiopure γ‐Butyrolactones via Tandem Knoevenagel‐Michael‐Lactonization Sequence en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Advanced Synthesis & Catalysis en_US
dc.publication.originofpublisher Foreign en_US


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