Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9328
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dc.contributor.authorMONDAL, SHANKHAJITen_US
dc.contributor.authorMALODE, AKHILESH NARENDRAen_US
dc.contributor.authorLONDHE, GOKUL S.en_US
dc.contributor.authorGNANAPRAKASAM, BOOPATHYen_US
dc.date.accessioned2025-02-28T05:17:14Z-
dc.date.available2025-02-28T05:17:14Z-
dc.date.issued2025-02en_US
dc.identifier.citationOrganic Lettersen_US
dc.identifier.issn1523-7060en_US
dc.identifier.issn1523-7052en_US
dc.identifier.urihttps://doi.org/10.1021/acs.orglett.4c04834en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9328-
dc.description.abstractHerein, 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.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectChemical reactionsen_US
dc.subjectElectromagnetic radiationen_US
dc.subjectIrradiationen_US
dc.subjectNitrogenen_US
dc.subjectPhotochemical reactionsen_US
dc.subject2025-FEB-WEEK1en_US
dc.subjectTOC-FEB-2025en_US
dc.subject2025en_US
dc.titleVisible Light-Induced Sequential Nitrogen Insertion and Benzotriazolation of Quinoxaline-2(1H)-onesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic Lettersen_US
dc.publication.originofpublisherForeignen_US
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