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One-Pot Synthesis of Pyrrolo[3,2-f]- and Pyrrolo[2,3-h]quinoline Derivatives: Observation of an Unexpected Mechanistic Pathway
| Content Provider | Semantic Scholar |
|---|---|
| Author | Ramesh, Subburethinam Nagarajan, Rajagopal |
| Copyright Year | 2012 |
| Abstract | SYNLETT 2012, 23, 717–722xx.xx.2012 Advanced online publication: 24.02.2012 DOI: 10.1055/s-0031-1290565; Art ID: B65611ST © Georg Thieme Verlag Stuttgart · New York Abstract: One-pot synthesis of pyrrolo[3,2-f]and pyrrolo[2,3h]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[2,3h]quinoline. |
| Starting Page | 717 |
| Ending Page | 722 |
| Page Count | 6 |
| File Format | PDF HTM / HTML |
| DOI | 10.1055/s-0031-1290565 |
| Volume Number | 23 |
| Alternate Webpage(s) | https://www.thieme-connect.de/media/synlett/201205/supmat/sup_b65611st-10-1055_s-0031-1290565.pdf |
| Alternate Webpage(s) | https://doi.org/10.1055/s-0031-1290565 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |