FeCl2-Catalyzed Rearrangement of Aryl Peroxyoxindole into 1,3-Benzooxazin-4-One

dc.contributor.author	MOHANTA, NIRMALA	en_US
dc.contributor.author	Samal, PragnyaParamita	en_US
dc.contributor.author	Krishnamurty, Sailaja	en_US
dc.contributor.author	GNANAPRAKASAM, BOOPATHY	en_US
dc.date.accessioned	2023-03-24T09:11:02Z
dc.date.available	2023-03-24T09:11:02Z
dc.date.issued	2023-02	en_US
dc.identifier.citation	Advanced Synthesis & Catalysis, 365(4), 515-521.	en_US
dc.identifier.issn	1615-4150	en_US
dc.identifier.issn	1615-4169	en_US
dc.identifier.uri	https://doi.org/10.1002/adsc.202201308	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/7675
dc.description.abstract	We report an FeCl2-catalyzed radical rearrangement of aryl peroxyoxindoles into 1,3-benzooxazin-2-ones to obtain a variety of aryl substituted 1,3-benzooxazin-4-ones in moderate to good yields. Mechanistically, this skeletal rearrangement of peroxyoxindoles proceeded via radical pathway and was well supported with a series of experimental findings and DFT studies.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.subject	Peroxyoxindole	en_US
dc.subject	FeCl2	en_US
dc.subject	Rearrangement	en_US
dc.subject	1,3-Benzooxazin-4-one	en_US
dc.subject	Ring expansion	en_US
dc.subject	2023-MAR-WEEK3	en_US
dc.subject	TOC-MAR-2023	en_US
dc.subject	2023	en_US
dc.title	FeCl2-Catalyzed Rearrangement of Aryl Peroxyoxindole into 1,3-Benzooxazin-4-One	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Advanced Synthesis & Catalysis	en_US
dc.publication.originofpublisher	Foreign	en_US