Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9482
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dc.contributor.authorSHAIKH, MOSEEN A.en_US
dc.contributor.authorUBALE, AKASH S.en_US
dc.contributor.authorGNANAPRAKASAM, BOOPATHYen_US
dc.date.accessioned2025-04-15T06:48:30Z-
dc.date.available2025-04-15T06:48:30Z-
dc.date.issued2024-02en_US
dc.identifier.citationJournal of Organic Chemistry, 89(04), 2283–2293.en_US
dc.identifier.issn0022-3263en_US
dc.identifier.issn1520-6904en_US
dc.identifier.urihttps://doi.org/10.1021/acs.joc.3c02260en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9482-
dc.description.abstractHerein, we have developed a continuous-process for the direct cyclopropanation of various alkenes nonconjugated with carbonyl using trimethylsulfoxonium iodide as a methylene source via the Corey–Chaykovsky cyclopropanation reaction in the presence of Amberlyst-A26 as a heterogeneous base. Several 9-alkylidene-9H-fluorene derivatives successfully undergo Corey–Chaykovsky cyclopropanation to afford spiro[cyclopropane-1,9′-fluorene] in excellent yields under the continuous-process module. Furthermore, continuous process for the cyclopropanation of 3-benzylideneindolin-2-one derivatives using Amberlyst-A26 as a heterogeneous base has been described, which afford spiro[cyclopropane-1,3′-indolin]-2′-one derivatives.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectAnionsen_US
dc.subjectColumn chromatographyen_US
dc.subjectCyclopropanationen_US
dc.subjectHydrocarbonsen_US
dc.subjectTransition temperatureen_US
dc.subject2024en_US
dc.titleAmberlyst-A26-Mediated Corey–Chaykovsky Cyclopropanation of 9-Alkylidene-9H-fluorene under Continuous Processen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleJournal of Organic Chemistryen_US
dc.publication.originofpublisherForeignen_US
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