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 |