Visible Light-Induced Sequential Nitrogen Insertion and Benzotriazolation of Quinoxaline-2(1H)-ones

GNANAPRAKASAM, BOOPATHY; LONDHE, GOKUL S.; MALODE, AKHILESH NARENDRA; MONDAL, SHANKHAJIT

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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