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Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3072
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dc.contributor.authorPARVATHALU, NENAVATHen_US
dc.contributor.authorAGALAVE, SANDIP G.en_US
dc.contributor.authorMOHANTA, NIRMALAen_US
dc.contributor.authorGNANAPRAKASAM, BOOPATHYen_US
dc.date.accessioned2019-05-30T11:41:43Z
dc.date.available2019-05-30T11:41:43Z
dc.date.issued2019-03en_US
dc.identifier.citationOrganic & Biomolecular Chemistry, 17(12), 3258-3266.en_US
dc.identifier.issn1477-0520en_US
dc.identifier.issn1477-0539en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3072-
dc.identifier.urihttps://doi.org/10.1039/c9ob00307jen_US
dc.description.abstractAn additive/Brønsted acid/base free, highly efficient and chemoselective transetherification of electron deficient vinylogous esters and water mediated de-alkylation using an earth-abundant Fe-catalyst under very mild reaction conditions is described. This reaction is highly selective to primary alcohols over secondary alcohols, has good functional group tolerance, is scalable to gram scale and a purification free sequential transetherification in a continuous flow mode is demonstrated.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectChemistryen_US
dc.subject2019en_US
dc.titleReversible chemoselective transetherification of vinylogous esters using Fe-catalyst under additive free conditionsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic & Biomolecular Chemistryen_US
dc.publication.originofpublisherForeignen_US
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