Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles

dc.contributor.author Prasad Tulichala, R. N.
dc.contributor.author Kumara Swamy, K. C.
dc.date.accessioned 2022-03-27T09:49:18Z
dc.date.available 2022-03-27T09:49:18Z
dc.date.issued 2015-08-04
dc.description.abstract Palladium catalysed-reaction of indole carboxylic acids with nitriles in the presence of Ag2CO3 proceeds via decarboxylative dual C-H activation leading to the nitrile insertion products, triazaindeno-fluorenes (indolocarbolines); in the absence of nitrile, diindolocarbazoles (heptacyclic triindoles or triazatruxenes) are formed.
dc.identifier.citation Chemical Communications. v.51(60)
dc.identifier.issn 13597345
dc.identifier.uri 10.1039/c5cc03160e
dc.identifier.uri http://xlink.rsc.org/?DOI=C5CC03160E
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13340
dc.title Palladium-catalysed decarboxylative nitrile insertion via C-H activation or self-coupling of indole-2-carboxylic acids: a new route to indolocarbolines and triindoles
dc.type Journal. Article
dspace.entity.type
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