1. Dspace@NITW
  2. Journal Papers
  3. Chemistry
Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3416
Full metadata record
DC FieldValueLanguage
dc.contributor.authorThunga, Sanjeeva-
dc.contributor.authorSingh, Neetika-
dc.contributor.authorInapanuri, Madhu-
dc.contributor.authorKokatla, Hari Prasad-
dc.date.accessioned2025-10-23T06:08:28Z-
dc.date.available2025-10-23T06:08:28Z-
dc.date.issued2024-
dc.identifier.citation10.1039/d4ob01356een_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/3416-
dc.descriptionNITWen_US
dc.description.abstractA rongalite-induced C(sp2)–H functionalization reaction has been developed for the synthesis of 3-(phenylsulfonylmethyl) indole derivatives from indole and arylsulfonyl hydrazides. This regioselective C–H functionalization provides a wide range of C-3 sulfonylmethyl indoles with upto 90% yields. Here, rongalite functions as a C1 unit source and a single electron donor. The use of inexpensive rongalite (ca. $0.03 per 1 g), mild reaction conditions and gram-scale synthesis are some of the key features of this methodology.en_US
dc.language.isoenen_US
dc.publisherOrganic & Biomolecular Chemistryen_US
dc.subjectRongaliteen_US
dc.titleRongalite induced metal-free C(sp2)–H functionalization of indoles: direct access to 3-(sulfonylmethyl) indolesen_US
dc.typeArticleen_US
Appears in Collections:Chemistry

Files in This Item:
File Description SizeFormat 
25. Org. Biomol. Chem., 2024, 22, 8787.pdf1.85 MBAdobe PDFView/Open
Show simple item record


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.