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DC Field | Value | Language |
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dc.contributor.author | MONDAL, SHANKHAJIT | en_US |
dc.contributor.author | MALODE, AKHILESH NARENDRA | en_US |
dc.contributor.author | LONDHE, GOKUL S. | en_US |
dc.contributor.author | GNANAPRAKASAM, BOOPATHY | en_US |
dc.date.accessioned | 2025-02-28T05:17:14Z | - |
dc.date.available | 2025-02-28T05:17:14Z | - |
dc.date.issued | 2025-02 | en_US |
dc.identifier.citation | Organic Letters | en_US |
dc.identifier.issn | 1523-7060 | en_US |
dc.identifier.issn | 1523-7052 | en_US |
dc.identifier.uri | https://doi.org/10.1021/acs.orglett.4c04834 | en_US |
dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9328 | - |
dc.description.abstract | Herein, we report a visible light-mediated sequential reaction involving in situ generation of benzotriazole from benzene-1,2-diamine and tert-butyl nitrite via nitrogen insertion and concomitant cross-coupling with quinoxaline-2(1H)-ones via C–N bond formation in one pot. This protocol uses metal-free mild conditions and demonstrated 36 examples of ≤80% yield with wide functional group tolerance. | en_US |
dc.language.iso | en | en_US |
dc.publisher | American Chemical Society | en_US |
dc.subject | Chemical reactions | en_US |
dc.subject | Electromagnetic radiation | en_US |
dc.subject | Irradiation | en_US |
dc.subject | Nitrogen | en_US |
dc.subject | Photochemical reactions | en_US |
dc.subject | 2025-FEB-WEEK1 | en_US |
dc.subject | TOC-FEB-2025 | en_US |
dc.subject | 2025 | en_US |
dc.title | Visible Light-Induced Sequential Nitrogen Insertion and Benzotriazolation of Quinoxaline-2(1H)-ones | 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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