One-pot synthesis of pyrrolo[3,2-f]-and pyrrolo[2,3-h]quinoline derivatives: Observation of an unexpected mechanistic pathway

dc.contributor.author Ramesh, Subburethinam
dc.contributor.author Nagarajan, Rajagopal
dc.date.accessioned 2022-03-27T08:40:20Z
dc.date.available 2022-03-27T08:40:20Z
dc.date.issued 2012-02-24
dc.description.abstract One-pot synthesis of pyrrolo[3,2-f]- and pyrrolo[2,3-h]quinolines were obtained starting from substituted 5-aminoindoles, benzaldehydes, and phenylacetylenes in the presence of La(OTf) 3 as a catalyst in good yields. The indole moiety in 5-aminoindole is believed to be mainly responsible for the observation of unexpected mechanistic pathway to the formation of pyrrolo[2,3-h]quinoline. © Georg Thieme Verlag Stuttgart · New York.
dc.identifier.citation Synlett. v.23(5)
dc.identifier.issn 09365214
dc.identifier.uri 10.1055/s-0031-1290565
dc.identifier.uri http://www.thieme-connect.de/DOI/DOI?10.1055/s-0031-1290565
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11445
dc.subject 5-aminoindole
dc.subject Lewis acid
dc.subject one-pot synthesis
dc.subject pyrroloquinoline
dc.title One-pot synthesis of pyrrolo[3,2-f]-and pyrrolo[2,3-h]quinoline derivatives: Observation of an unexpected mechanistic pathway
dc.type Journal. Review
dspace.entity.type
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