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

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/4672

Full metadata record

DC Field	Value	Language
dc.contributor.author	Yadav, Hare Ram	-
dc.contributor.author	Choudhury, Angshuman R.	-
dc.date.accessioned	2023-08-14T06:48:14Z	-
dc.date.available	2023-08-14T06:48:14Z	-
dc.date.issued	2022	-
dc.identifier.citation	Chemical Communications, 58(84), 11827-11830	en_US
dc.identifier.uri	https://doi.org/10.1039/d2cc04273h	-
dc.identifier.uri	http://hdl.handle.net/123456789/4672	-
dc.description	Only IISERM authors are available in the record	en_US
dc.description.abstract	Herein, 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.language.iso	en_US	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	cascade reaction	en_US
dc.subject	isocyanide insertion	en_US
dc.subject	indolylisoindolinones	en_US
dc.title	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	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

Files in This Item:

File	Description	Size	Format
Need To Add…Full Text_PDF.		15.36 kB	Unknown	View/Open