Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10198
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dc.contributor.authorHOSSAIN, MD JABEDen_US
dc.contributor.authorSHAH, BRIJ KUMARen_US
dc.contributor.authorDash, Soumya Ranjanen_US
dc.contributor.authorKASHISHen_US
dc.contributor.authorVanka, Kumaren_US
dc.contributor.authorKHAN, SHABANAen_US
dc.date.accessioned2025-06-24T11:45:09Z-
dc.date.available2025-06-24T11:45:09Z-
dc.date.issued2025-03en_US
dc.identifier.citationChemistry—A European Journal, 31(13).en_US
dc.identifier.issn1521-3765en_US
dc.identifier.issn0947-6539en_US
dc.identifier.urihttps://doi.org/10.1002/chem.202403449en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10198-
dc.description.abstractIn this work, we have reduced CO2 with HBpin to afford borylated methanol product selectively in ~99 % yield using Ce[N(SiMe3)2]3(THF)3 as a catalyst. This led to multigram scale isolation of methanol obtained from CO2 reduction via the hydrolysis of borylated methanol, this establishes the potential of Ce[N(SiMe3)2]3(THF)3 as an efficient homogeneous catalyst for the bulk scale methanol synthesis. A practical application of this catalytic system was also shown by reducing CO2-containing motorbike exhaust efficiently and selectively. Further, C−O bond activation of esters and epoxides using HBpin and 1–2 mol % of Ce[N(SiMe3)2]3(THF)3 at 60 °C afforded the borylated alcohols in good to excellent yields, which can easily be hydrolysed to the eco-friendly corresponding alcohol. The stoichiometric experiments were performed to prove the formation of in-situ generated cerium hydride [Ce]-H as an active catalyst.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subject2025en_US
dc.titleCe[N(SiMe3)2]3(THF)3-Catalyzed Hydroboration of CO2, Esters and Epoxides with Pinacolborane: Selective Synthesis of Methanol in Multigram Scaleen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemistry—A European Journalen_US
dc.publication.originofpublisherForeignen_US
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