Reactivity of alkynylindole-2-carboxamides in [Pd]-catalysed C-H activation and phase transfer catalysis: Formation of pyrrolo-dIIndolones: Vs. β-carbolinones

dc.contributor.author Tulichala, R. N.Prasad
dc.contributor.author Swamy, K. C.Kumara
dc.date.accessioned 2022-03-27T09:49:11Z
dc.date.available 2022-03-27T09:49:11Z
dc.date.issued 2016-01-01
dc.description.abstract The divergent behaviour of 3-alkynylindole-2-carboxamides, under palladium catalysed conditions and phase-transfer catalytic conditions, is described. Thus, palladium catalysed intramolecular C-N and C-C bond formation in a single step by C-H activation involving 3-alkynylindole-2-carboxamides and leading to pyrrolodIIndolones in high yields is developed. In contrast, using the same precursors, a high yielding regio- and chemo-selective route for 3-substituted β-carbolinones by phase-transfer catalysis is established via intramolecular C-N bond formation. The structures of key products are confirmed by X-ray crystallography.
dc.identifier.citation Organic and Biomolecular Chemistry. v.14(19)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/c6ob00583g
dc.identifier.uri http://xlink.rsc.org/?DOI=C6OB00583G
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13338
dc.title Reactivity of alkynylindole-2-carboxamides in [Pd]-catalysed C-H activation and phase transfer catalysis: Formation of pyrrolo-dIIndolones: Vs. β-carbolinones
dc.type Journal. Article
dspace.entity.type
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