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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | CHAUDHARI, MORESHWAR B. | en_US |
| dc.contributor.author | CHAUDHARY, ATUL | en_US |
| dc.contributor.author | KUMAR, VISHNUPRIYA | en_US |
| dc.contributor.author | GNANAPRAKASAM, BOOPATHY | en_US |
| dc.date.accessioned | 2019-03-26T10:01:40Z | |
| dc.date.available | 2019-03-26T10:01:40Z | |
| dc.date.issued | 2019-02 | en_US |
| dc.identifier.citation | Organic Letters, 21(06),1617-1621. | en_US |
| dc.identifier.issn | 1523-7060 | en_US |
| dc.identifier.issn | 1523-7052 | en_US |
| dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2407 | - |
| dc.identifier.uri | https://doi.org/10.1021/acs.orglett.9b00155 | en_US |
| dc.description.abstract | An unprecedented skeletal rearrangement of 3-(tert-butylperoxy)indolin-2-one using a tin catalyst has been developed. This rearrangement is highly selective to afford a series of fluorophoric (Z)-2-arylidene and alkylidene-An unprecedented skeletal rearrangement of 3-(tert-butylperoxy)indolin-2-one using a tin catalyst has been developed. This rearrangement is highly selective to afford a series of fluorophoric (Z)-2-arylidene and alkylidene-2H-benzo[b][1,4]oxazin-3(4H)-one derivatives in good to excellent yield. In contrast with Sn(OTf)2, the reaction of 3-(tert-butylperoxy)indolin-2-one derivatives with FeCl3 afforded the Hock fragmentation product via C–C bond cleavage. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | TOC-MAR-2019 | en_US |
| dc.subject | 2019 | en_US |
| dc.title | The Rearrangement of Peroxides for the Construction of Fluorophoric 1,4-Benzoxazin-3-one Derivatives | en_US |
| dc.type | Article | en_US |
| dc.contributor.department | Dept. of Chemistry | en_US |
| dc.identifier.sourcetitle | Organic Letters | en_US |
| dc.publication.originofpublisher | Foreign | en_US |
| Appears in Collections: | JOURNAL ARTICLES | |
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