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Amberlyst-A26-Mediated Corey–Chaykovsky Cyclopropanation of 9-Alkylidene-9H-fluorene under Continuous Process

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dc.contributor.author SHAIKH, MOSEEN A. en_US
dc.contributor.author UBALE, AKASH S. en_US
dc.contributor.author GNANAPRAKASAM, BOOPATHY en_US
dc.date.accessioned 2025-04-15T06:48:30Z
dc.date.available 2025-04-15T06:48:30Z
dc.date.issued 2024-02 en_US
dc.identifier.citation Journal of Organic Chemistry, 89(04), 2283–2293. en_US
dc.identifier.issn 0022-3263 en_US
dc.identifier.issn 1520-6904 en_US
dc.identifier.uri https://doi.org/10.1021/acs.joc.3c02260 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9482
dc.description.abstract Herein, 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.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Anions en_US
dc.subject Column chromatography en_US
dc.subject Cyclopropanation en_US
dc.subject Hydrocarbons en_US
dc.subject Transition temperature en_US
dc.subject 2024 en_US
dc.title Amberlyst-A26-Mediated Corey–Chaykovsky Cyclopropanation of 9-Alkylidene-9H-fluorene under Continuous Process en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Journal of Organic Chemistry en_US
dc.publication.originofpublisher Foreign en_US


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