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