A cascade reaction of indolyl-migratory isocyanide insertion, scaffold rearrangement and redox-neutral event with isocyanide as a C(sp3)H–N synthon efficiently constructs indolylisoindolinones

dc.contributor.authorYadav, Hare Ram
dc.contributor.authorChoudhury, Angshuman R.
dc.date.accessioned2023-08-14T06:48:14Z
dc.date.available2023-08-14T06:48:14Z
dc.date.issued2022
dc.descriptionOnly IISERM authors are available in the recorden_US
dc.description.abstractHerein, we report a Pd(0)-catalyzed cascade reaction of intramolecular indolyl isocyanide-insertion, isocyanide-initiated scaffold-rearrangement with indolyl migration and redox-neutral process, which affords an efficient access to indolylisoindolinones. Isocyanide as a C(sp3)H–N synthon and the alkyl motif of isocyanide as a hydride source have been explored for the first time.en_US
dc.identifier.citationChemical Communications, 58(84), 11827-11830en_US
dc.identifier.urihttps://doi.org/10.1039/d2cc04273h
dc.identifier.urihttp://hdl.handle.net/123456789/4672
dc.language.isoen_USen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectcascade reactionen_US
dc.subjectisocyanide insertionen_US
dc.subjectindolylisoindolinonesen_US
dc.titleA cascade reaction of indolyl-migratory isocyanide insertion, scaffold rearrangement and redox-neutral event with isocyanide as a C(sp3)H–N synthon efficiently constructs indolylisoindolinonesen_US
dc.typeArticleen_US

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